JP6132656B2 - Method for producing picene and derivatives thereof - Google Patents

Description

  The present invention provides a method for producing picene and derivatives thereof that can be used in applications such as organic semiconductors, organic thin film transistors, organic field effect transistors, or organic solar cells. Furthermore, the present invention provides a method for producing picene and derivatives thereof, which are increasingly useful for these applications, with a short reaction process with high yield.

Conventionally, pentacene is known as an organic semiconductor material, and Patent Documents 1 and 2 propose use of pentacene as an organic semiconductor. However, pentacene has a drawback of low stability in the atmosphere. Therefore, Non-Patent Document 1 reports an organic TFT using a condensed aromatic ring having a structure in which a benzene ring is bent like picene. Since picene has a lower ionization potential than pentacene, it is described that the compound has excellent oxidation stability in the atmosphere, and can be said to be extremely advantageous when used as an organic semiconductor.
According to Example 1 of Patent Document 3, picene was synthesized in a yield of 3% by a 5-step reaction. According to another experiment of Example 1 of Patent Document 3, a 3-step reaction was performed. The synthesis of picene with a yield of 5% is not reasonable because of the large number of steps and low yield.

JP-A-5-55568 JP 2001-94107 A WO2010 / 016511

H. Okamoto et al., “Air-assisted High-performance Field-effect Transistor with Thin Films of Picene” (Journal of the American Chemical Society), [online], July 16, 2008 Web Release, American Chemical Society, [ Search on August 6, 2008], Internet <URL: http://pubs.acs.org/cgi-bin/abstract.cgi/jacsat/asap/abs/ja803291a.html>

Accordingly, an object of the present invention is to provide a method for producing picene and derivatives thereof, which are increasingly useful in applications such as organic semiconductors, organic thin film transistors, organic field effect transistors, or organic solar cells, in a high yield by a short reaction process. There is to do.
Another object of the present invention is to provide a novel compound useful as an intermediate for picene and its derivatives.

As a result of intensive studies to achieve the above object, the present inventor obtained picene and its derivatives in a high yield in two steps from the compounds represented by the following general formula (2) and the following general formula (3). The present invention has been completed by finding that it can be manufactured.
That is, the present invention relates to the following [1] to [13].
According to the present invention, picene and its derivatives can be produced in a relatively high yield by a reaction of only two steps. In addition, according to the present invention, picene and its derivatives can be produced with a high yield under mild conditions.
The picene and its derivative manufactured by this invention can be used for uses, such as an organic semiconductor, a field effect transistor, an organic thin-film transistor, and an organic thin-film solar cell.
The picene and its derivatives produced in the present invention have a lower ionization potential than pentacene, so that the oxidation stability of the compound in the atmosphere is excellent, and it is extremely advantageous when used as an organic semiconductor.

[1] A compound (b) represented by the following general formula (2) and a compound (c) represented by the following general formula (3) are subjected to a coupling reaction, thereby being represented by the following general formula (1). Step 1 for producing the compound (a) to be produced;
And a process 2 for dehydrohalogenating the compound (a) represented by the following general formula (1), and a method for producing a picene represented by the following general formula (4) and a derivative thereof.

（式中、Ｘ₁及びＸ₂はハロゲン原子を示し、Ｒ₇及びＲ₈はそれぞれ独立に水素原子、ハロゲン原子、ニトロ基、保護されていてもよい水酸基、保護されていてもよいアミノ基、保護されるか又は塩を形成していてもよいカルボキシル基、置換基を有していてもよい炭素数１〜２０の炭化水素基、置換基を有していてもよい炭素数１〜２０のアルコキシ基又は−ＳｉＲ₁₃Ｒ₁₄Ｒ₁₅で表される基を示し、Ｒ₁₃、Ｒ₁₄及びＲ₁₅はそれぞれ独立に水素原子又は置換基を有していてもよい炭素数１〜２０の炭化水素基を示す。）

(Wherein X ₁ and X ₂ represent a halogen atom, R ₇ and R ₈ each independently represent a hydrogen atom, a halogen atom, a nitro group, an optionally protected hydroxyl group, an optionally protected amino group, A carboxyl group that may be protected or may form a salt, a hydrocarbon group having 1 to 20 carbon atoms that may have a substituent, and a carbon group having 1 to 20 carbon atoms that may have a substituent An alkoxy group or a group represented by —SiR ₁₃ R ₁₄ R ₁₅ , wherein R ₁₃ , R ₁₄ and R ₁₅ are each independently a hydrogen atom or a hydrocarbon having 1 to 20 carbon atoms which may have a substituent; Group.)

（式中、Ａｒは、アリール基を表し、Ａｒ中の水素原子は、ハロゲン原子、ニトロ基、保護されていてもよい水酸基、保護されていてもよいアミノ基、保護されるか又は塩を形成していてもよいカルボキシル基、置換基を有していてもよい炭素数１〜２０の炭化水素基、置換基を有していてもよい炭素数１〜２０のアルコキシ基又は−ＳｉＲ₁₃Ｒ₁₄Ｒ₁₅により置換されていてもよく、Ｒ₅及びＲ₆はそれぞれ独立に水素原子、ハロゲン原子、ニトロ基、保護されていてもよい水酸基、保護されていてもよいアミノ基、保護されるか又は塩を形成していてもよいカルボキシル基、置換基を有していてもよい炭素数１〜２０の炭化水素基、置換基を有していてもよい炭素数１〜２０のアルコキシ基又は−ＳｉＲ₁₃Ｒ₁₄Ｒ₁₅で表される基を示し、Ｒ₁₁及びＲ₁₂はそれぞれ独立に水素原子又は炭素数１〜２０のアルコキシ基を示し、Ｒ₁₁及びＲ₁₂は環を形成していてもよく、Ｒ₁₃、Ｒ₁₄及びＲ₁₅はそれぞれ独立に水素原子又は置換基を有していてもよい炭素数１〜２０の炭化水素基を示す。）

(In the formula, Ar represents an aryl group, and a hydrogen atom in Ar is a halogen atom, a nitro group, an optionally protected hydroxyl group, an optionally protected amino group, protected or forms a salt. An optionally substituted carboxyl group, an optionally substituted hydrocarbon group having 1 to 20 carbon atoms, an optionally substituted alkoxy group having 1 to 20 carbon atoms, or —SiR ₁₃ R _14. R ₁₅ may be substituted, and R ₅ and R ₆ are each independently a hydrogen atom, a halogen atom, a nitro group, an optionally protected hydroxyl group, an optionally protected amino group, protected or A carboxyl group which may form a salt, a hydrocarbon group having 1 to 20 carbon atoms which may have a substituent, an alkoxy group having 1 to 20 carbon atoms which may have a substituent, or -SiR ₁₃ represents a group represented by R ₁₄ R _{15, 11} and R ₁₂ independently represent a hydrogen atom or an alkoxy group having a carbon number of 1 to 20, R ₁₁ and R ₁₂ may form a ring, R _13, R ₁₄ and R ₁₅ independently represent hydrogen (The C1-C20 hydrocarbon group which may have an atom or a substituent is shown.)

（式中、Ｘ₁はハロゲン原子を示し、Ａｒ、Ｒ₅及びＲ₆は上記一般式（３）と同一であり、Ｒ₇及びＲ₈は上記一般式（２）と同一であり、２つあるＡｒ、Ｒ₅又はＲ₆は互いに異なっていてもよく、Ａｒ中の水素原子は、上記一般式（３）と同様に置換されていてもよい。）

(Wherein X ₁ represents a halogen atom, Ar, R ₅ and R ₆ are the same as in the above general formula (3), R ₇ and R ₈ are the same as in the above general formula (2), Ar, R ₅ or R ₆ may be different from each other, and the hydrogen atom in Ar may be substituted in the same manner as in the general formula (3).

（式中、Ａｒ、Ｒ₅及びＲ₆は上記一般式（３）と同一であり、２つあるＡｒ、Ｒ₅又はＲ₆は互いに異なっていてもよく、Ａｒ中の水素原子は、上記一般式（３）と同様に置換されていてもよい。）

(In the formula, Ar, R ₅ and R ₆ are the same as in the general formula (3), two Ar, R ₅ or R ₆ may be different from each other, and the hydrogen atom in Ar is (It may be substituted in the same manner as in formula (3).)

[2] The process for producing picene and derivatives thereof according to [1], wherein the reaction in step 1 is performed in the presence of a catalyst comprising a transition metal compound and a tri-substituted phosphine and a base.
[3] The transition metal compound used in Step 1 is selected from the group consisting of palladium compounds, rhodium compounds, platinum compounds, nickel compounds, cobalt compounds, copper compounds, iron compounds, iridium compounds, ruthenium compounds, silver compounds and gold compounds. The method for producing picene and derivatives thereof according to [2], which is at least one transition metal compound.
[4] The picene and the derivative thereof according to [2] or [3], wherein the trisubstituted phosphine used in Step 1 is at least one trisubstituted phosphine selected from the group consisting of trialkylphosphine and triarylphosphine. Production method.
[5] The method for producing picene and derivatives thereof according to any one of [2] to [4], wherein the base used in step 1 is potassium hydroxide or sodium hydroxide.

[6] The process for producing picene and derivatives thereof according to [1] or [2], wherein the reaction of step 2 is performed in the presence of a catalyst comprising a transition metal compound and trisubstituted phosphine and a base.
[7] The transition metal compound used in step 2 is selected from the group consisting of palladium compounds, rhodium compounds, platinum compounds, nickel compounds, cobalt compounds, copper compounds, iron compounds, iridium compounds, ruthenium compounds, silver compounds and gold compounds. The method for producing picene and derivatives thereof according to [6], which is at least one transition metal compound.
[8] The trisubstituted phosphine used in Step 2 is at least one trisubstituted phosphine selected from the group consisting of a tricycloalkylphosphine, a trialkylphosphine, and a triarylphosphine, according to [6] or [7] A process for producing picene and its derivatives.
[9] The method for producing picene and derivatives thereof according to any one of [6] to [8], wherein the base used in step 2 is an alkali metal carbonate.

[10] An organic semiconductor comprising picene produced by the production method according to any one of [1] to [9] and a derivative thereof.
[11] A field effect transistor comprising picene produced by the production method according to any one of [1] to [9] and a derivative thereof.
[12] A solar cell comprising picene produced by the production method according to any one of [1] to [9] and a derivative thereof.

  [13] A compound represented by the following general formula (1).

（式中、Ｘ₁はハロゲン原子を示し、Ａｒ、Ｒ₅及びＲ₆は上記一般式（３）と同一であり、Ｒ₇及びＲ₈は上記一般式（２）と同一であり、２つあるＡｒ、Ｒ₅又はＲ₆は互いに異なっていてもよく、Ａｒ中の水素原子は、上記一般式（３）と同様に置換されていてもよい。）

(Wherein X ₁ represents a halogen atom, Ar, R ₅ and R ₆ are the same as in the above general formula (3), R ₇ and R ₈ are the same as in the above general formula (2), Ar, R ₅ or R ₆ may be different from each other, and the hydrogen atom in Ar may be substituted in the same manner as in the general formula (3).

According to the present invention, picene and its derivatives can be produced in a high yield under a small number of steps and mild conditions.
The picene and its derivative manufactured by this invention can be used for uses, such as an organic semiconductor, a field effect transistor, an organic thin-film transistor, and an organic thin-film solar cell.
The picene and its derivatives produced in the present invention have a lower ionization potential than pentacene, so that the oxidation stability of the compound in the atmosphere is excellent, and it is extremely advantageous when used as an organic semiconductor.

Hereinafter, the present invention will be described in detail, but the present invention is not limited thereto.
First, the production method of the present invention will be described.
<Step 1: Synthesis of halogen-substituted precursor>
In step 1, a compound (b) represented by the following general formula (2) and a compound (c) represented by the following general formula (3) are subjected to a coupling reaction, whereby the following general formula (1) The compound (a) represented is produced.

（式中、Ｘ₁及びＸ₂はハロゲン原子を示し、Ｒ₇及びＲ₈はそれぞれ独立に水素原子、ハロゲン原子、ニトロ基、保護されていてもよい水酸基、保護されていてもよいアミノ基、保護されるか又は塩を形成していてもよいカルボキシル基、置換基を有していてもよい炭素数１〜２０の炭化水素基、置換基を有していてもよい炭素数１〜２０のアルコキシ基又は−ＳｉＲ₁₃Ｒ₁₄Ｒ₁₅で表される基を示し、Ｒ₁₃、Ｒ₁₄及びＲ₁₅はそれぞれ独立に水素原子又は置換基を有していてもよい炭素数１〜２０の炭化水素基を示す。）

(Wherein X ₁ and X ₂ represent a halogen atom, R ₇ and R ₈ each independently represent a hydrogen atom, a halogen atom, a nitro group, an optionally protected hydroxyl group, an optionally protected amino group, A carboxyl group that may be protected or may form a salt, a hydrocarbon group having 1 to 20 carbon atoms that may have a substituent, and a carbon group having 1 to 20 carbon atoms that may have a substituent An alkoxy group or a group represented by —SiR ₁₃ R ₁₄ R ₁₅ , wherein R ₁₃ , R ₁₄ and R ₁₅ are each independently a hydrogen atom or a hydrocarbon having 1 to 20 carbon atoms which may have a substituent; Group.)

（式中、Ａｒは、アリール基を表し、Ａｒ中の水素原子は、ハロゲン原子、ニトロ基、保護されていてもよい水酸基、保護されていてもよいアミノ基、保護されるか又は塩を形成していてもよいカルボキシル基、置換基を有していてもよい炭素数１〜２０の炭化水素基、置換基を有していてもよい炭素数１〜２０のアルコキシ基又は−ＳｉＲ₁₃Ｒ₁₄Ｒ₁₅により置換されていてもよく、Ｒ₅及びＲ₆はそれぞれ独立に水素原子、ハロゲン原子、ニトロ基、保護されていてもよい水酸基、保護されていてもよいアミノ基、保護されるか又は塩を形成していてもよいカルボキシル基、置換基を有していてもよい炭素数１〜２０の炭化水素基、置換基を有していてもよい炭素数１〜２０のアルコキシ基又は−ＳｉＲ₁₃Ｒ₁₄Ｒ₁₅で表される基を示し、Ｒ₁₁及びＲ₁₂はそれぞれ独立に水素原子又は炭素数１〜２０のアルコキシ基を示し、Ｒ₁₁及びＲ₁₂は環を形成していてもよく、Ｒ₁₃、Ｒ₁₄及びＲ₁₅はそれぞれ独立に水素原子又は置換基を有していてもよい炭素数１〜２０の炭化水素基を示す。）

(In the formula, Ar represents an aryl group, and a hydrogen atom in Ar is a halogen atom, a nitro group, an optionally protected hydroxyl group, an optionally protected amino group, protected or forms a salt. An optionally substituted carboxyl group, an optionally substituted hydrocarbon group having 1 to 20 carbon atoms, an optionally substituted alkoxy group having 1 to 20 carbon atoms, or —SiR ₁₃ R _14. R ₁₅ may be substituted, and R ₅ and R ₆ are each independently a hydrogen atom, a halogen atom, a nitro group, an optionally protected hydroxyl group, an optionally protected amino group, protected or A carboxyl group which may form a salt, a hydrocarbon group having 1 to 20 carbon atoms which may have a substituent, an alkoxy group having 1 to 20 carbon atoms which may have a substituent, or -SiR ₁₃ represents a group represented by R ₁₄ R _{15, 11} and R ₁₂ independently represent a hydrogen atom or an alkoxy group having a carbon number of 1 to 20, R ₁₁ and R ₁₂ may form a ring, R _13, R ₁₄ and R ₁₅ independently represent hydrogen (The C1-C20 hydrocarbon group which may have an atom or a substituent is shown.)

（式中、Ｘ₁はハロゲン原子を示し、Ａｒ、Ｒ₅及びＲ₆は上記一般式（３）と同一であり、Ｒ₇及びＲ₈は上記一般式（２）と同一であり、２つあるＡｒ、Ｒ₅又はＲ₆は互いに異なっていてもよく、Ａｒ中の水素原子は、上記一般式（３）と同様に置換されていてもよい。）

(Wherein X ₁ represents a halogen atom, Ar, R ₅ and R ₆ are the same as in the above general formula (3), R ₇ and R ₈ are the same as in the above general formula (2), Ar, R ₅ or R ₆ may be different from each other, and the hydrogen atom in Ar may be substituted in the same manner as in the general formula (3).

In the general formulas (1) and (3), Ar represents an aryl group, and examples of the aryl group include an aromatic hydrocarbon ring and an aromatic heterocycle.
Examples of the aromatic hydrocarbon ring include a benzene ring, and examples of the aromatic heterocycle include a thiophene ring, a furan ring, a selenophene ring, a tellurophen ring, a pyrrole ring, an imidazole ring, a pyrazole ring, a tellurazole ring, and an isotelrazole ring. , A selenazole ring, an isoselenazole ring, a thiazole ring, an isothiazole ring, an oxazole ring, an isoxazole ring, a furazane ring, and the like.

In the general formulas (1) to (3), R ₅ , R ₆ , R ₇ and R ₈ are each independently a hydrogen atom, a halogen atom, a nitro group, an optionally protected hydroxyl group or a protected group. An amino group which may be protected, a carboxyl group which may be protected or form a salt, a hydrocarbon group having 1 to 20 carbon atoms which may have a substituent, and a substituent; A C 1-20 alkoxy group or a group represented by —SiR ₁₃ R ₁₄ R ₁₅ , wherein R ₁₃ , R ₁₄ and R ₁₅ may each independently have a hydrogen atom or a substituent; A hydrocarbon group having 1 to 20 carbon atoms is shown. X ₁ and X _{2 each} represent a halogen atom.
Examples of the halogen atom include fluorine, chlorine, bromine, iodine, etc. The hydroxyl group which may be protected includes, in addition to the hydroxyl group, carbon number 1 such as acetyloxy group, propionyloxy group, acryloyl group, methacryloyl group and the like. ˜20 alkylcarbonyloxy groups can be exemplified. The amino group which may be protected has a substituent having 1 to 20 carbon atoms such as ethylamino group, propylamino group, diethylamino group, dipropylamino group, hexylamino group and dicyclopentylamino group. The amino group which may be sufficient can be illustrated. Examples of the carboxyl group that may be protected or may form a salt include carboxyl groups, carboxylates formed by carboxyl groups with various bases, esters having 1 to 20 carbon atoms formed with various alcohols, and the like. be able to. Examples of the optionally substituted hydrocarbon group having 1 to 20 carbon atoms include methyl group, ethyl group, propyl group, propenyl group, butyl group, butenyl group, pentyl group, hexyl group, cyclopentyl group, and cyclohexyl group. And a hydrocarbon group such as a cyclohexenyl group and a group in which these hydrocarbon groups are substituted. Examples of the alkoxy group having 1 to 20 carbon atoms which may have a substituent include alkoxy groups such as a methoxy group, an ethoxy group, a propoxy group and a butoxy group, and groups in which these alkoxy groups are substituted. Can do.
Examples of BR ₁₁ R ₁₂ include various boronic acids such as boronic acid, boronic acid catechol ester, and boronic acid pinacol ester, and ester residues thereof. R ₁₁ and R ₁₂ are the same as described above. R ₁₁ and R ₁₂ may form a ring.

As the compound (b) represented by the general formula (2), the following compounds are preferable.
The compound whose R < ₇ > and R < ₈ > is a hydrogen atom or a C1-C20 hydrocarbon group.
A compound in which X ₁ and X ₂ are a chlorine atom, a bromine atom, or an iodine atom.
Moreover, as a compound (c) represented by the said General formula (3), the following compounds are preferable.
A compound in which the hydrogen atom of Ar is not substituted, or the hydrogen atom of Ar is protected by a hydrocarbon group having 1 to 20 carbon atoms or a protected hydroxyl group (particularly, protected by a hydrocarbon group having 1 to 20 carbon atoms) A compound substituted with a group represented by (hydroxyl group) or —SiR ₁₃ R ₁₄ R ₁₅ .
A compound in which R ₅ and R ₆ are a hydrogen atom or a hydrocarbon group having 1 to 20 carbon atoms.
A compound in which the group represented by BR ₁₁ R ₁₂ is a boronic acid pinacol ester.
Therefore, the following compounds are preferred as the compound (a) represented by the general formula (1).
A compound in which the hydrogen atom of Ar is not substituted, or the hydrogen atom of Ar is protected by a hydrocarbon group having 1 to 20 carbon atoms or a protected hydroxyl group (particularly, protected by a hydrocarbon group having 1 to 20 carbon atoms) A compound substituted with a group represented by (hydroxyl group) or —SiR ₁₃ R ₁₄ R ₁₅ .
A compound in which R ₅ and R ₆ are a hydrogen atom or a hydrocarbon group having 1 to 20 carbon atoms.
The compound whose R < ₇ > and R < ₈ > is a hydrogen atom or a C1-C20 hydrocarbon group.
A compound in which X ₁ is a chlorine atom, a bromine atom, or an iodine atom.

<Reaction and reaction conditions in step 1>
The reaction in Step 1 is carried out by performing a coupling reaction between the compound (b) represented by the general formula (2) and the compound (c) represented by the general formula (3) from a transition metal compound and a trisubstituted phosphine. In the presence of a catalyst and a base.
The usage-amount of the compound (b) represented by the said General formula (2) and the compound (c) represented by the said General formula (3) is the mole with respect to the compound (b) represented by the said General formula (2). The ratio is usually 0.3 to 3.0, preferably 0.5 to 2.0.
The transition metal compound is at least one selected from the group consisting of palladium compounds, rhodium compounds, platinum compounds, nickel compounds, cobalt compounds, copper compounds, iron compounds, iridium compounds, ruthenium compounds, silver compounds, and gold compounds. Transition metal compounds are exemplified. The transition metal compound may be a halide, nitrate, acetate, acetylacetonate complex or the like of each compound described above.
Among the transition metal compounds, palladium compounds are preferable from the viewpoint of activity.
Examples of the tri-substituted phosphine include tritert-butylphosphine, trisec-butylphosphine, n-butylphosphine, tripropylphosphine, trihexylphosphine, etc. And triarylphosphine such as tolylphosphine.
As the base, potassium hydroxide or sodium hydroxide is preferably used. The usage-amount of a base is 1-20 as a molar ratio with respect to the compound (b) represented by the said General formula (2), Preferably it is 3-8.
The reaction of Step 1 is usually performed in the presence of a solvent. As the solvent, ethers such as diethyl ether, tetrahydrofuran, and dioxane are usually used, and the amount used is appropriate.
Reaction of the process 1 is normally implemented at the temperature of -20-70 degreeC, Preferably it is 0-50 degreeC, and reaction time is 1 to 50 hours normally, Preferably it is 3 to 30 hours.

<Step 2: Synthesis of picene and derivatives thereof>
In step 2, picene and its derivative represented by the following general formula (4) are produced by dehydrohalogenating the compound (a) represented by the above general formula (1).

（式中、Ａｒ、Ｒ₅及びＲ₆は上記一般式（３）と同一であり、２つあるＡｒ、Ｒ₅又はＲ₆は互いに異なっていてもよく、Ａｒ中の水素原子は、上記一般式（３）と同様に置換されていてもよい。）

(In the formula, Ar, R ₅ and R ₆ are the same as in the general formula (3), two Ar, R ₅ or R ₆ may be different from each other, and the hydrogen atom in Ar is (It may be substituted in the same manner as in formula (3).)

In the general formula (4), examples of the group represented by Ar, R ₅ , R ₆ , R ₇ and R ₈ are the same as those exemplified in Step 1.

<Reaction and reaction conditions in step 2>
The reaction of step 2 is carried out in the presence of a catalyst comprising a transition metal compound and a tri-substituted phosphine and a base.
The transition metal compound is at least one selected from the group consisting of palladium compounds, rhodium compounds, platinum compounds, nickel compounds, cobalt compounds, copper compounds, iron compounds, iridium compounds, ruthenium compounds, silver compounds, and gold compounds. Transition metal compounds are exemplified. The transition metal compound may be a halide, nitrate, acetate, acetylacetonate complex or the like of each compound described above.
Examples of the tri-substituted phosphine include tritert-butylphosphine, trisec-butylphosphine, n-butylphosphine, tripropylphosphine, trihexylphosphine, etc. And triarylphosphine such as tolylphosphine.
Among the transition metal compounds, palladium compounds are preferable from the viewpoint of activity.
As the base, alkali metal carbonates or alkaline earth metal carbonates can be preferably used. Specifically, potassium carbonate, sodium carbonate, potassium hydrogen carbonate, sodium hydrogen carbonate, potassium hydroxide, sodium hydroxide, etc. Is mentioned. The usage-amount of a base is 1-20 as a molar ratio with respect to General formula (1), Preferably it is 3-8. Further, it is preferably carried out in the presence of silver nitrate.
The reaction of step 2 is usually performed in the presence of a solvent. As the solvent, nonpolar solvents such as dimethylformamide and dimethylsulfoxide, and ether solvents such as diethyl ether, tetrahydrofuran and dioxane are usually used, and the amount used is appropriate.
Reaction of the process 2 is normally implemented at the temperature of 0-200 degreeC, Preferably it is 50-150 degreeC, and reaction time is 1 to 50 hours normally, Preferably it is 3 to 30 hours.

<Uses of picene and its derivatives>
The picene and its derivative manufactured by this invention can be used for an organic semiconductor, a field effect transistor or an organic thin-film transistor, an organic thin-film solar cell, etc.
The picene and its derivatives produced in the present invention have a lower ionization potential than pentacene, so that the oxidation stability of the compound in the atmosphere is excellent, and it is extremely advantageous when used as an organic semiconductor.

Next, the novel compound of the present invention will be described. In addition, about the point which is not demonstrated especially, the description in the manufacturing method of this invention is applied suitably.
The novel compound of the present invention is represented by the following general formula (1).

（式中、Ｘ₁はハロゲン原子を示し、Ａｒ、Ｒ₅及びＲ₆は上記一般式（３）と同一であり、Ｒ₇及びＲ₈は上記一般式（２）と同一であり、２つあるＡｒ、Ｒ₅又はＲ₆は互いに異なっていてもよく、Ａｒ中の水素原子は、上記一般式（３）と同様に置換されていてもよい。）

(Wherein X ₁ represents a halogen atom, Ar, R ₅ and R ₆ are the same as in the above general formula (3), R ₇ and R ₈ are the same as in the above general formula (2), Ar, R ₅ or R ₆ may be different from each other, and the hydrogen atom in Ar may be substituted in the same manner as in the general formula (3).

In the general formula (1), Ar, as the _{R 5, R 6, R 7} , a group represented by R ₈ and X _1, the same thing can be mentioned as illustrative in step 1 of the production method of the present invention.
Moreover, the preferable compound of the compound represented by the said General formula (1) and its manufacturing method are as having mentioned above.

  The present invention will be specifically described below with reference to examples. The present invention is not limited to this example.

[Reference Example 1] Synthesis of 1,4-dibromo-2,3-diiodobenzene

1,3-ジヨードベンゼン(化合物９,6.6ｇ,20mmol)をジエチルエーテル(50ml)に溶解し、-78℃に冷却した。攪拌させながら１０分かけてn-ブチルリチウム(12.3ml,20mmol,1.63Mヘキサン溶液)を添加したところオフホワイトの溶液が得られた。-78℃のまま１時間攪拌した後、トリメチルシシリルクロライド(2.39g,22mmol)を加え、室温で４時間攪拌した。反応溶液に水(10ml)を加え、有機層をジエチルエーテルで抽出した。抽出液を飽和食塩水で洗浄し、無水硫酸マグネシウムで脱水した。ろ過後、ろ液を減圧下で濃縮することにより、褐色油状物(化合物１０)を得た。
200mlの二口丸底フラスコに、上記で得られた化合物１０(5.5g,19.9mmol)、ビス（トリフェニルホスフィン）パラジウム(II)ジクロライド（Pd(PPh₃)₂Cl₂,140mg,0.2mmol)、ヨウ化銅(190mg,1.0mmol)、トリエチルアミン(70ml)及びトリメチルシリルアセチレン(3.37ml,23.8mmol)をアルゴン雰囲気下で仕込み、室温で12時間攪拌した。トリエチルアミンを減圧留去し、残渣をジエチルエーテルを用いてろ過した。ろ液を減圧留去することで褐色油状物(化合物１１,4.5g,収率92%)を得た。
得られた化合物１１(4.5g,18.2mmol)をテトラヒドロフラン(50ml)及びメタノール(30ml)の混合溶媒に溶解し、水(1.5ml)に溶解した炭酸カリウム(3.78g,27.3mmol)を添加し、室温で4.5時間攪拌した。反応溶液に飽和塩化アンモニウム水溶液及びジエチルエーテルを加えた。有機層を5%-塩化アンモニウム水溶液及び飽和食塩水で洗浄し、硫酸マグネシウムで乾燥させた。有機層を減圧留去して、フロリジルにより精製することで、褐色油状物（化合物１２,2.47g,収率86％）を得た。
50mlのシュレンク管にクロロ(1,5-シクロオクタジエン)ロジウム(I)ダイマー(0.058g,0.12mmol)を仕込んだ後、アルゴンを流した。シクロヘキサン(25ml)、トリイソプロピルフェニル(0.090ml,0.47mmol),トリエチルアミン(6ml)及び4,4,5,5-テトラメチル-1,3,2-ジオキサボロラン(1.14ml,7.85mmol)を連続して加え、15℃にて30分間攪拌した後、上記で得られた化合物１２(2.74g,15.7mmol)を一度に加え、室温で攪拌しながら2時間反応させ、その後、メタノールを加えた。反応液をろ過及び減圧留去して、粗生成物を得た。これを蒸留精製して、褐色油状物（化合物１３,2.09g,収率88%)を得た。生成物が目的物であることは、¹H-NMRで確認した。 [Reference Example 2] Synthesis of TMS- (Z) -alkenylboronic acid ester

1,3-Diiodobenzene (Compound 9,6.6 g, 20 mmol) was dissolved in diethyl ether (50 ml) and cooled to -78 ° C. N-Butyllithium (12.3 ml, 20 mmol, 1.63 M hexane solution) was added over 10 minutes with stirring to obtain an off-white solution. After stirring at −78 ° C. for 1 hour, trimethylsilylsilyl chloride (2.39 g, 22 mmol) was added, and the mixture was stirred at room temperature for 4 hours. Water (10 ml) was added to the reaction solution, and the organic layer was extracted with diethyl ether. The extract was washed with saturated brine and dehydrated over anhydrous magnesium sulfate. After filtration, the filtrate was concentrated under reduced pressure to obtain a brown oil (Compound 10).
In a 200 ml two-necked round bottom flask, compound 10 (5.5 g, 19.9 mmol) obtained above, bis (triphenylphosphine) palladium (II) dichloride (Pd (PPh ₃ ) ₂ Cl ₂ , 140 mg, 0.2 mmol) , Copper iodide (190 mg, 1.0 mmol), triethylamine (70 ml) and trimethylsilylacetylene (3.37 ml, 23.8 mmol) were charged in an argon atmosphere and stirred at room temperature for 12 hours. Triethylamine was distilled off under reduced pressure, and the residue was filtered using diethyl ether. The filtrate was evaporated under reduced pressure to give a brown oil (compound 11,4.5 g, yield 92%).
The obtained compound 11 (4.5 g, 18.2 mmol) was dissolved in a mixed solvent of tetrahydrofuran (50 ml) and methanol (30 ml), potassium carbonate (3.78 g, 27.3 mmol) dissolved in water (1.5 ml) was added, Stir at room temperature for 4.5 hours. A saturated aqueous ammonium chloride solution and diethyl ether were added to the reaction solution. The organic layer was washed with 5% aqueous ammonium chloride solution and saturated brine, and dried over magnesium sulfate. The organic layer was distilled off under reduced pressure and purified by Florisil to obtain a brown oil (compound 12,2.47 g, yield 86%).
A 50 ml Schlenk tube was charged with chloro (1,5-cyclooctadiene) rhodium (I) dimer (0.058 g, 0.12 mmol) and then flushed with argon. Cyclohexane (25 ml), triisopropylphenyl (0.090 ml, 0.47 mmol), triethylamine (6 ml) and 4,4,5,5-tetramethyl-1,3,2-dioxaborolane (1.14 ml, 7.85 mmol) in succession. In addition, after stirring at 15 ° C. for 30 minutes, the compound 12 (2.74 g, 15.7 mmol) obtained above was added all at once and reacted at room temperature with stirring for 2 hours, and then methanol was added. The reaction solution was filtered and evaporated under reduced pressure to obtain a crude product. This was purified by distillation to give a brown oil (compound 13,2.09 g, yield 88%). It was confirmed by ¹ H-NMR that the product was the desired product.

¹ H NMR (CDCl3, 300 MHz, rt): δ 0.31 (s, 9H), 1.31 (s, 12H), 5.61 (d, J = 14.7 Hz, 1H), 7.23 (d, J = 14.7 Hz, 1H) , 7.26-7.35 (m, 1H), 7.45 (d, J = 9.6 Hz, 1H), 7.56 (d, J = 10.5 Hz, 1H), 7.82 (s, 1H).

20 mLのシュレンク管にアルゴン雰囲気下で、ビス（ジベンジリデン）パラジウム(57.5mg,0.10mmol,20mol%), トリ（ターシャリーブチル）ホスフィン (0.4mL, 0.5M, 0.20mmol,40mol%)と1,4-ジブロモ-2,3-ジヨードベンゼン(化合物５, 243mg, 0.5mmol)のテトラヒドロフラン(4 mL)溶液を調製した。そこへ、(Z)-アルケニルボロン酸エステル(化合物６,230mg,1.0mmol)と水酸化カリウム(168mg,3mmol)を室温で加えた。反応混合物を室温で１２時間撹拌したのち、さらに、(Z)-アルケニルボロン酸エステル(化合物７, 92mg,0.4mmol)を加えた。さらに室温で１２時間撹拌したのち、反応混合物を1 Mの塩酸に注ぎ、反応を停止させた。その後、反応溶液を分液ロートに移し、ジエチルエーテル(10mL)で２回抽出した。抽出液を飽和食塩水で洗浄し、無水硫酸マグネシウムで脱水した。ろ過後、ろ液を減圧下で濃縮することにより、茶色の油状物質を得た。これをヘキサンを溶離液として、シリカゲルカラムクロマトグラフィーで精製することにより、白色固体として、目的化合物７を64mg、収率30%で得た。目的化合物７が得られていることは、¹Ｈ−ＮＭＲ、ＵＶスペクトル及び質量分析により確認した。 [Example 1]
<Step 1> Suzuki-Miyaura coupling reaction of 1,4-dibromo-2,3-diiodobenzene and (Z) -alkenylboronic acid ester

In a 20 mL Schlenk tube under argon atmosphere, bis (dibenzylidene) palladium (57.5 mg, 0.10 mmol, 20 mol%), tri (tertiary butyl) phosphine (0.4 mL, 0.5 M, 0.20 mmol, 40 mol%) and 1 , 4-Dibromo-2,3-diiodobenzene (Compound 5, 243 mg, 0.5 mmol) in tetrahydrofuran (4 mL) was prepared. Thereto, (Z) -alkenylboronic acid ester (Compound 6,230 mg, 1.0 mmol) and potassium hydroxide (168 mg, 3 mmol) were added at room temperature. After the reaction mixture was stirred at room temperature for 12 hours, (Z) -alkenylboronic acid ester (Compound 7, 92 mg, 0.4 mmol) was further added. After further stirring for 12 hours at room temperature, the reaction mixture was poured into 1 M hydrochloric acid to stop the reaction. The reaction solution was then transferred to a separatory funnel and extracted twice with diethyl ether (10 mL). The extract was washed with saturated brine and dehydrated over anhydrous magnesium sulfate. After filtration, the filtrate was concentrated under reduced pressure to obtain a brown oily substance. This was purified by silica gel column chromatography using hexane as an eluent to obtain 64 mg of the target compound 7 as a white solid in a yield of 30%. It was confirmed by ¹ H-NMR, UV spectrum, and mass spectrometry that the target compound 7 was obtained.

¹ H NMR (CDCl ₃ , 300 MHz, rt) δ 6.01 (d, J = 12 Hz, 2H), 6,46 (d, J = 12 Hz, 2H), 6.92-6.97 (m, 4H), 7.12- 7.20 (m, 6H), 7.43 (s, 2H)
FT-IR (KBr, cm ^-1 ): 3055 (m), 3024 (m), 1492 (s), 1448 (m), 1427 (m), 1383 (w), 1113 (s), 1026 (m) , 960 (m), 868 (m), 839 (m), 804 (s), 772 (m), 750 (m), 692 (s)
MS (EI, m / z (relative intensity)): 440 (M +, 11), 351 (13), 347 (14), 282 (11), 280 (16), 276 (12), 202 (34), 189 (20), 167 (60), 91 (100)
UV-Vis (1.0 × 10 ^-3 g / L, CHCl ₃ ): 251nm

20mLのシュレンク管にアルゴン雰囲気下で、ジクロロ（ジアセトニトリル）パラジウム(18.4mg,0.048mmol,40mol%),トリシクロヘキシルホスフィン((27mg,0.096mmol)とN,N-ジメチルホルムアミド (DMA)(2mL)を加えた。１０分間撹拌したのち、反応混合物に対して炭酸セシウム(78mg,0.24mmol)、ピバル酸(5.0 mg,0.048mmol, 40mol%)及び化合物７ (53mg, 0.12mmol)を室温で加えた。反応混合物を135度で 24時間加熱したのち、室温まで冷まし、1Mの塩酸3mLを加えることにより反応を停止した。その後、反応溶液を分液ロートに移し、ジクロロメタン(10mL)で２回抽出した。抽出液を飽和食塩水で洗浄し、無水硫酸マグネシウムで脱水した。ろ過後、ろ液を減圧下で濃縮した。これをクロロホルムを溶離液として、高速液体クロマトグラフィー（HPLC）で精製することにより、くすんだ白色固体として、目的化合物８を12 mg、収率36%で得た。目的化合物８が得られていることは、¹Ｈ−ＮＭＲ、ＵＶスペクトル及び質量分析により確認した。 <Step 2> Synthesis of picene

Dichloro (diacetonitrile) palladium (18.4 mg, 0.048 mmol, 40 mol%), tricyclohexylphosphine ((27 mg, 0.096 mmol) and N, N-dimethylformamide (DMA) (2 mL) in a 20 mL Schlenk tube under argon atmosphere After stirring for 10 minutes, cesium carbonate (78 mg, 0.24 mmol), pivalic acid (5.0 mg, 0.048 mmol, 40 mol%) and compound 7 (53 mg, 0.12 mmol) were added to the reaction mixture at room temperature. The reaction mixture was heated at 135 ° C. for 24 hours, then cooled to room temperature and quenched by adding 3 mL of 1M hydrochloric acid, then the reaction solution was transferred to a separatory funnel and extracted twice with dichloromethane (10 mL). The extract was washed with saturated brine, dehydrated with anhydrous magnesium sulfate, filtered, and the filtrate was concentrated under reduced pressure, and purified by high performance liquid chromatography (HPLC) using chloroform as an eluent. Dull white solid As, to the desired compound 8 12 mg, was obtained in 36% yield. The object compound 8 is obtained, ¹ H-NMR, it was confirmed by UV spectrum and mass spectrometry.

¹ H NMR (CDCl ₃ , 300 MHz, rt) δ 7.68 (q, J = 9 Hz, 2H), 7.74 (q, J = 9 Hz, 2H), 8.00-8.06 (m, 4H), 8.80 (d, J = 9 Hz, 2H), 8.87 (d, J = 9 Hz, 2H), 8.97 (s, 2H)
FT-IR (KBr, cm ^-1 ): 1263 (m), 1134 (w), 1024 (w), 945 (w), 806 (s), 754 (s), 738 (s), 526 (m)
MS (EI, m / z (relative intensity)): 278 (M +, 100), 277 (12), 276 (27), 139 (20), 138 (18)
UV-Vis (1.0 × 10 ^-3 g / L, CHCl ₃ , nm): 258, 276, 286, 303, 314, 328

20 mLのシュレンク管にアルゴン雰囲気下で、1,4-ジクロロ-2,3-ジヨードベンゼン(化合物１４, 176mg, 0.44mmol)、[1,3-ビス(2,6-ジイソプロピルフェニル)イミダゾール-2-イリデン](3-クロロピリジル)パラジウム(II)ジクロリド(PEPPSI-IPr,27mg,0.04mmol), TMS-(Z)-アルケニルボロン酸エステル(化合物１３,292mg,0.97mmol)及び水酸化カリウム(148mg,2.64mmol)を混合した。そこへ、トルエン(5ml)及び水(1ml)を加え、110℃で12時間反応させた。反応混合物を室温まで冷却し、1N−塩酸で反応を停止させた。その後、反応溶液を分液ロートに移し、ジエチルエーテル(10mL)で２回抽出した。抽出液を飽和食塩水で洗浄し、無水硫酸マグネシウムで脱水した。ろ過後、ろ液を減圧下で濃縮することにより、茶色油状物を得た。これをヘキサンを溶離液として、シリカゲルカラムクロマトグラフィーで精製することにより、茶色油状物として、目的化合物１５を0.15g、収率68%で得た。目的化合物１５が得られていることは、¹Ｈ−ＮＭＲ、及び¹³Ｃ−ＮＭＲにより確認した。 [Example 2]
<Step 1> Suzuki-Miyaura coupling reaction of 1,4-dichloro-2,3-diiodobenzene and TMS- (Z) -alkenylboronic acid ester

In a 20 mL Schlenk tube under an argon atmosphere, 1,4-dichloro-2,3-diiodobenzene (compound 14, 176 mg, 0.44 mmol), [1,3-bis (2,6-diisopropylphenyl) imidazole- 2-Ilidene] (3-chloropyridyl) palladium (II) dichloride (PEPPSI-IPr, 27 mg, 0.04 mmol), TMS- (Z) -alkenylboronic acid ester (compound 13,292 mg, 0.97 mmol) and potassium hydroxide ( 148 mg, 2.64 mmol) were mixed. Toluene (5 ml) and water (1 ml) were added thereto and reacted at 110 ° C. for 12 hours. The reaction mixture was cooled to room temperature and quenched with 1N hydrochloric acid. The reaction solution was then transferred to a separatory funnel and extracted twice with diethyl ether (10 mL). The extract was washed with saturated brine and dehydrated over anhydrous magnesium sulfate. After filtration, the filtrate was concentrated under reduced pressure to obtain a brown oil. This was purified by silica gel column chromatography using hexane as an eluent to obtain 0.15 g of the target compound 15 as a brown oil in a yield of 68%. It was confirmed by ¹ H-NMR and ¹³ C-NMR that the objective compound 15 was obtained.

¹ H NMR (CDCl ₃ , 300 MHz, rt) δ 0.14 (s, 18H), 6.03 (d, J = 12.0 Hz, 2H), 6.53 (d, J = 12.3 Hz, 2H), 7.02 (s, 2H) , 7.11 (s, 2H), 7.21 (m, 2H), 7.32-7.35 (m, 4H). ¹³ C NMR (CDCl ₃ , 75 MHz, rt) δ -1.39, -1.14, 125.48, 127.71, 128.86, 129.10 , 132.30, 132.34, 132.81, 135.94, 137.50, 140.19.

20mLのシュレンク管にアルゴン雰囲気下で、ジクロロ（ジアセトニトリル）パラジウム(11.9mg,0.031mmol,10mol%),トリシクロヘキシルホスフィン(17.3mg,0.062mmol)とN,N-ジメチルホルムアミド(2mL)を加えた。１０分間撹拌したのち、反応混合物に対して炭酸セシウム(202mg,0.62mmol)、ピバル酸(12.7mg,0.12mmol, 40mol%)及び化合物１５(156mg, 0.31mmol)を室温で加えた。反応混合物を150度で 20時間加熱したのち、室温まで冷まし、1Mの塩酸3mLを加えることにより反応を停止した。その後、反応溶液を分液ロートに移し、ジクロロメタン(10mL)で３回抽出した。抽出液を飽和食塩水で洗浄し、無水硫酸マグネシウムで脱水した。ろ過後、ろ液を減圧下で濃縮した。再結晶法により精製し、オフホワイト色の目的化合物１６(60mg,収率47%)で得た。目的化合物１６が得られていることは、¹Ｈ−ＮＭＲ、¹³Ｃ−ＮＭＲ、ＦＴ−ＩＲスペクトル、質量分析及びＵＶ−Ｖｉｓスペクトルにより確認した。 <Step 2> Synthesis of 3,10-bis (trimethylsilyl) picene

Dichloro (diacetonitrile) palladium (11.9 mg, 0.031 mmol, 10 mol%), tricyclohexylphosphine (17.3 mg, 0.062 mmol) and N, N-dimethylformamide (2 mL) were added to a 20 mL Schlenk tube under an argon atmosphere. . After stirring for 10 minutes, cesium carbonate (202 mg, 0.62 mmol), pivalic acid (12.7 mg, 0.12 mmol, 40 mol%) and compound 15 (156 mg, 0.31 mmol) were added to the reaction mixture at room temperature. The reaction mixture was heated at 150 degrees for 20 hours, then cooled to room temperature and quenched by adding 3 mL of 1M hydrochloric acid. Thereafter, the reaction solution was transferred to a separatory funnel and extracted three times with dichloromethane (10 mL). The extract was washed with saturated brine and dehydrated over anhydrous magnesium sulfate. After filtration, the filtrate was concentrated under reduced pressure. The product was purified by recrystallization and obtained as the off-white target compound 16 (60 mg, 47% yield). It was confirmed by ¹ H-NMR, ¹³ C-NMR, FT-IR spectrum, mass spectrometry and UV-Vis spectrum that the target compound 16 was obtained.

¹ H NMR (CDCl ₃ , 300 MHz, rt) δ 0.41 (s, 18H), 7.87 (d, J = 9.1 Hz, 2H), 8.04 (d, J = 9.3 Hz, 2H), 8.16 (s, 2H) , 8.81 (q, J = 9.0 Hz, 4H), 8.96 (s, 2H).
¹³ C NMR (CDCl ₃ , 75 MHz, rt) δ 0.81, 121.82, 122.37, 127.81, 128.72, 128.89, 128.99, 130.95, 131.32, 131.44, 134.41, 138.96
FT-IR (KBr, cm ^-1 ): 1248 (m), 1111 (w), 910 (w), 839 (m), 810 (s), 758 (m).
MS (EI, m / z (relative intensity)): 422 (M +, 100), 409 (13), 408 (36), 407 (85), 196 (49), 73 (62).
UV-Vis: ε = 1.5 × 10 ⁵ L ・ mol ^-1・ cm ^-1
c = 1.0 × 10 ^-3 g / L = 2.37 × 10 ^-6 mol / L (solvent: CHCl ₃ )

1,4-ジクロロ-2,3-ジヨードベンゼン(化合物１４)及び(Z)-4,4,5,5-テトラメチル-2-(2-フェニル-1-ブテン-1-イル）-1,3,2-ジオキサボロラン(化合物１７)とから、実施例２の工程１と同様の手法により、黄色油状物の目的化合物１８(収率67%）を得た。目的化合物１８が得られていることは、各種分析により確認した。 [Example 3]
<Step 1> 1,4-Dichloro-2,3-diiodobenzene and (Z) -4,4,5,5-tetramethyl-2- (2-phenyl-1-buten-1-yl) -1 Suzuki-Miyaura coupling reaction of 1,3,2-dioxaborolane

1,4-dichloro-2,3-diiodobenzene (compound 14) and (Z) -4,4,5,5-tetramethyl-2- (2-phenyl-1-buten-1-yl) -1 , 3,2-Dioxaborolane (Compound 17) was prepared in the same manner as in Step 1 of Example 2 to give the target compound 18 (yield 67%) as a yellow oil. It was confirmed by various analyzes that the target compound 18 was obtained.

FT-IR (neat, cm ^-1 ): 2965 (s), 2929 (s), 2359 (s), 1427 (m), 1150 (m), 806 (w), 772 (m), 698 (s) .
¹ H NMR (CDCl ₃ , 600 MHz, rt) δ 1.04 (t, J = 7.2 Hz, 6H), 2.48-2.54 (m, 4H), 5.46 (s, 2H), 6.91-6.97 (m, 4H), 7.06 (s, 2H), 7.10-7.18 (m, 6H)
¹³ C [ ¹ H] NMR (CDCl ₃ , 150 MHz, rt) δ 13.1, 31.1, 122.0, 126.9, 127.6, 127.7, 127.7, 127.8, 127.8, 132.5, 137.9, 140.5.
MS (EI, m / z (relative intensity)): 407 (M +, 7), 406 (24), 377 (26), 289 (24), 252 (23), 119 (43), 117 (40), 105 (39), 91 (100).
HRMS (EI) Calcd for C ₂₆ H ₂₄ Cl ₂ : 406.1255. Found: 406.1263.

化合物１８から、実施例２の工程２と同様の手法により、白色固体の目的化合物１９(収率30%)を得た。目的化合物１９が得られていることは、各種分析により確認した。尚、質量分析については、目的化合物１９の沸点が高いため検出されなかった。 <Step 2> Synthesis of 5,8-diethylpicene

The target compound 19 (yield 30%) as a white solid was obtained from the compound 18 by the same method as in Step 2 of Example 2. It was confirmed by various analyzes that the target compound 19 was obtained. Mass spectrometry was not detected because the target compound 19 had a high boiling point.

Mp.> 300 ° C.
FT-IR (KBr, cm ^-1 ): 2926 (m), 1452 (w), 1248 (w), 1042 (w), 876 (m), 746 (s).
¹ H NMR (CDCl ₃ , 300 MHz, rt) δ 1.57 (t, J = 8.1 Hz, 6H), 3.35 (q, J = 18 Hz, 4H), 7.66-7.76 (m, 4H), 8.23 (q, J = 6.0 Hz, 2H), 8.65 (s, 2H), 8.87 (s, 2H), 8.91 (q, J = 9.0 Hz, 2H)
¹³ C [ ¹ H] NMR (CDCl ₃ , 75 MHz, rt) δ 15.2, 27.1, 120.2, 120.8, 123.7, 124.3, 126.2, 126.4, 127.9, 128.1, 130.9, 131.0, 138.9.

1,4-ジクロロ-2,3-ジヨードベンゼン(化合物１４)及び(Z)-2-(3-メトキシスチリル)-4,4,5,5-テトラメチル-1,3,2-ジオキサボロラン(化合物２０)とから、実施例２の工程１と同様の手法により、黄色油状物の目的化合物２１(収率67%）を得た。目的化合物２１が得られていることは、各種分析により確認した。 [Example 4]
<Step 1> of 1,4-dichloro-2,3-diiodobenzene and (Z) -2- (3-methoxystyryl) -4,4,5,5-tetramethyl-1,3,2-dioxaborolane Suzuki-Miyaura coupling reaction

1,4-dichloro-2,3-diiodobenzene (compound 14) and (Z) -2- (3-methoxystyryl) -4,4,5,5-tetramethyl-1,3,2-dioxaborolane ( Compound 20) was used to give the target compound 21 (yield 67%) as a yellow oil in the same manner as in Step 1 of Example 2. It was confirmed by various analyzes that the target compound 21 was obtained.

FT-IR (neat, cm ^-1 ): 2938 (w), 1597 (s), 1578 (s), 1489 (s), 1435 (s), 1260 (s), 1153 (m), 1042 (s) , 860 (w), 795 (s), 689 (m).
¹ H NMR (CDCl ₃ , 300 MHz, rt) δ 3.60 (s, 6H), 6.10 (d, = 12 Hz, 2H), 6.49 (d, J = 3.9 Hz, 3H), 6.55 (t, J = 6.6 Hz, 3H), 6.68-6.75 (m, 2H), 7.05-7.10 (m, 2H), 7.31 (s, 2H)
¹³ C [ ¹ H] NMR (CDCl ₃ , 75 MHz, rt) δ 54.9, 112.9, 113.6, 119.3, 124.0, 125.6, 128.7, 129.1, 129.2, 132.2, 133.2, 136.0, 137.4, 138.0.
MS (EI, m / z (relative intensity)): 411 (M +, 5), 410 (19), 302 (16), 289 (27), 227 (79), 121 (100), 91 (14).
Anal. Calcd for C ₂₄ H ₂₀ Cl ₂ O ₂ : C, 70.08; H, 4.90%. Found: C, 69.93; H, 4.78%.

化合物２１から、実施例２の工程２と同様の手法により、白色固体の目的化合物２２(収率24%)を得た。目的化合物２２が得られていることは、各種分析により確認した。尚、質量分析については、目的化合物２２の沸点が高いため検出されなかった。 <Step 2> Synthesis of 3,10-dimethoxypicene

The target compound 22 (yield 24%) as a white solid was obtained from the compound 21 by the same method as in Step 2 of Example 2. It was confirmed by various analyzes that the target compound 22 was obtained. Mass spectrometry was not detected because the target compound 22 had a high boiling point.

Mp.> 300 ° C.
FT-IR (KBr, cm ^-1 ): 2930 (w), 1522 (m), 1450 (s), 1427 (s), 1269 (s), 1238 (s), 1140 (s), 1059 (s) , 841 (s), 820 (s), 748 (s), 704 (w).
¹ H NMR (CDCl ₃ , 600 MHz, rt) δ 4.21 (s, 6H), 7.21 (q, J = 12 Hz, 2H), 7.58-7.64 (m, 4H), 7.96 (d, J = 9.6 Hz, 2H), 8.83 (d, J = 9.0 Hz, 2H), 9.92 (s, 2H)
¹³ C [ ¹ H] NMR (CDCl ₃ , 150 MHz, rt) δ 55.9, 108.2, 121.1, 121.4, 122.5, 126.5, 126.6, 127.1, 128.5, 128.8, 134.3, 158.9.

1,4-ジクロロ-2,3-ジヨードベンゼン(化合物１４)及び(Z)-2-(2,4-ジメトキシスチリル)-4,4,5,5-テトラメチル-1,3,2-ジオキサボロラン(化合物２３)とから、実施例２の工程１と同様の手法により、黄色油状物の目的化合物２４(収率38%）を得た。目的化合物２４が得られていることは、各種分析により確認した。 [Example 5]
<Step 1> 1,4-Dichloro-2,3-diiodobenzene and (Z) -2- (2,4-dimethoxystyryl) -4,4,5,5-tetramethyl-1,3,2- Suzuki-Miyaura coupling reaction of dioxaborolane

1,4-dichloro-2,3-diiodobenzene (compound 14) and (Z) -2- (2,4-dimethoxystyryl) -4,4,5,5-tetramethyl-1,3,2- The target compound 24 (38% yield) as a yellow oil was obtained from dioxaborolane (Compound 23) in the same manner as in Step 1 of Example 2. It was confirmed by various analyzes that the target compound 24 was obtained.

FT-IR (neat, cm ^-1 ): 2938 (w), 1608 (s), 1503 (s), 1464 (w), 1292 (s), 1290 (s), 1159, (s), 823 (w ).
¹ H NMR (CDCl ₃ , 300 MHz, rt) δ 3.76 (s, 6H), 3.80 (s, 6H), 6.17 (q, J = 8.7 Hz, 2H), 6.36 (s, 2H), 6.57 (q, J = 7.5 Hz, 2H), 6.78 (d, J = 12 Hz, 2H), 7.23 (s, 2H), 7.29 (s, 2H)
¹³ C [ ¹ H] NMR (CDCl ₃ , 75 MHz, rt) δ 55.0, 55.4, 98.1, 104.1, 119.0, 123.5, 128.5, 128.9, 131.9, 137.9, 157.9, 160.3.
MS (EI, m / z (relative intensity)): 471 (M +, 7), 470 (26), 332 (12), 151 (100), 121 (16).
HRMS (EI) Calcd for C ₂₆ H ₂₄ Cl ₂ O ₄ : 470.1052. Found: 470.1043.

化合物２４から、実施例２の工程２と同様の手法により、白色固体の目的化合物２５(収率31%)を得た。目的化合物２５が得られていることは、各種分析により確認した。 <Step 2> Synthesis of 2,4,9,11-tetramethoxypicene

The target compound 25 (yield 31%) as a white solid was obtained from the compound 24 in the same manner as in Step 2 of Example 2. It was confirmed by various analyzes that the target compound 25 was obtained.

Mp.> 300 ° C.
FT-IR (KBr, cm ^-1 ): 2999 (w), 1618 (s), 1454 (m), 1416 (m), 1383 (m), 1261 (s), 1148 (s), 1047 (s) , 808 (m), 644 (w).
¹ H NMR (CDCl ₃ , 600 MHz, rt) δ 4.06 (s, 6H), 4.08 (s, 6H), 6.70 (d, J = 2.4 Hz, 2H), 7.73 (d, J = 1.8 Hz, 2H) , 8.37 (d, J = 9.6 Hz, 2H), 8.64 (d, J = 9.0 Hz, 2H), 8.74 (s, 2H)
¹³ C [ ¹ H] NMR (CDCl ₃ , 150 MHz, rt) δ 55.7, 56.0, 95.5, 97.9, 118.9, 119.2, 121.1, 121.6, 127.9, 129.8, 132.6, 157.3, 159.3.
HRMS (EI) Calcd for C ₂₆ H ₂₂ O ₄ : 398.1518, Found: 398.1502.

1,4-ジクロロ-2,3-ジヨードベンゼン(化合物１４)及び(Z)-2-(3-デシルスチリル)-4,4,5,5-テトラメチル-1,3,2-ジオキサボロラン(化合物２６)とから、実施例２の工程１と同様の手法により、黄色油状物の目的化合物２７(収率75%）を得た。目的化合物２７が得られていることは、各種分析により確認した。 [Example 6]
<Step 1> Suzuki of 1,4-dichloro-2,3-diiodobenzene and (Z) -2- (3-decylstyryl) -4,4,5,5-tetramethyl-1,3,2-dioxaborolane -Miyaura coupling reaction

1,4-dichloro-2,3-diiodobenzene (compound 14) and (Z) -2- (3-decylstyryl) -4,4,5,5-tetramethyl-1,3,2-dioxaborolane (compound) 26) and the target compound 27 (yield 75%) as a yellow oil was obtained in the same manner as in Step 1 of Example 2. It was confirmed by various analyzes that the target compound 27 was obtained.

FT-IR (neat, cm ^-1 ): 2924 (s), 2853 (s), 2357 (w), 1600 (w), 1456 (m), 1435 (m), 1128 (m), 903 (w) , 804 (s), 696 (s).
¹ H NMR (CDCl ₃ , 300 MHz, rt) δ 0.87-0.91 (m, 6H), 1.26-1.31 (m, 32H), 2.43 (t, J = 7.7 Hz, 4H), 6.00 (d, J = 12.0 Hz, 2H), 6.49 (d, J = 12.0 Hz, 2H), 6.77 (d, J = 12.0 Hz, 4H), 6.96 (d, J = 7.5 Hz, 2H), 7.07 (t, J = 7.5 Hz, 2), 7.29 (s, 2H)
¹³ C [ ¹ H] NMR (CDCl ₃ , 75 MHz, rt) δ 14.1, 22.7, 29.2, 29.4, 29.5, 29.6, 29.7, 31.2, 31.9, 35.7, 125.3, 125.4, 125.7, 128.0, 128.1, 128.1, 129.0 , 132.2, 136.7, 137.5, 142.7.

化合物２７から、実施例２の工程２と同様の手法により、白色固体の目的化合物２８(収率20%)を得た。目的化合物２８が得られていることは、各種分析により確認した。 <Step 2> Synthesis of 3,10-didecylpicene

The target compound 28 (yield 20%) as a white solid was obtained from the compound 27 in the same manner as in Step 2 of Example 2. It was confirmed by various analyzes that the target compound 28 was obtained.

Mp.> 300 ° C.
FT-IR (KBr, cm ^-1 ): 1713 (w), 1466 (w), 1263 (w), 1096 (m), 785 (m), 507 (m).
¹ H NMR (CDCl ₃ , 600 MHz, rt) δ 0.86-0.89 (m, 6H), 1.25-1.44 (m, 28H), 1.75-1.80 (m, 4H), 2.86 (t, 4H), 7,58 (q, J = 6 Hz, 2H), 7.78 (s, 2H), 7.97 (d, J = 9.0 Hz, 2H), 8.75 (q, J = 12 Hz, 4H), 8.90 (s, 2H)
¹³ C [ ¹ H] NMR (CDCl ₃ , 150 MHz, rt) δ 14.1, 22.7, 29.3, 29.4, 29.6, 29.6, 29.6, 31.5, 31.9, 35.9, 121.5, 121.6, 123.0, 127.2, 127.3, 128.0, 128.2 , 128.5, 128.7, 132.0, 141.3.

1,4-ジクロロ-2,3-ジヨードベンゼン(化合物１４)及び(Z)-4,4,5,5-テトラメチル-2-(2-(チオフェン-3-イル）ビニル）-1,3,2-ジオキサボロラン(化合物２９)とから、実施例２の工程１と同様の手法により、橙色油状物の目的化合物３０(収率48%）を得た。目的化合物３０が得られていることは、各種分析により確認した。 [Example 7]
<Step 1> 1,4-Dichloro-2,3-diiodobenzene and (Z) -4,4,5,5-tetramethyl-2- (2- (thiophen-3-yl) vinyl) -1, Suzuki-Miyaura coupling reaction of 3,2-dioxaborolane

1,4-dichloro-2,3-diiodobenzene (compound 14) and (Z) -4,4,5,5-tetramethyl-2- (2- (thiophen-3-yl) vinyl) -1, The target compound 30 (48% yield) as an orange oil was obtained from 3,2-dioxaborolane (Compound 29) in the same manner as in Step 1 of Example 2. It was confirmed by various analyzes that the target compound 30 was obtained.

FT-IR (neat, cm ^-1 ): 2926 (s), 1724 (s), 1634 (w), 1435 (s), 1281 (s), 1265 (m), 1125 (s), 870 (m) , 797 (s), 773 (m).
¹ H NMR (300 MHz, 25 oC, CDCl ₃ ): 6.08 (d, J = 12.0 Hz, 2H), 6.56-6.60 (m, 4H), 6.91 (d, J = 2.4 Hz, 2H), 7.09-7.11 (m, 2H), 7.37 (s, 1H).
¹³ C [ ¹ H] NMR (75 MHz, 25 oC, CDCl ₃ ): 124.0, 124.3, 125.4, 126.4, 127.0, 129.4, 132.3, 137.8, 138.0
MS (EI, m / z (relative intensity)): 363 (M +, 11), 362 (15), 280 (11), 278 (16), 267 (17), 265 (25), 258 (11), 208 (14), 179 (40), 97 (100).

化合物３０から、実施例２の工程２と同様の手法により、黄白色固体の目的化合物３１(収率38%)を得た。目的化合物３１が得られていることは、各種分析により確認した。 <Step 2> Synthesis of 5,8-diethylpicene

The target compound 31 (yield 38%) as a pale yellow solid was obtained from the compound 30 by the same method as in Step 2 of Example 2. It was confirmed by various analyzes that the target compound 31 was obtained.

mp 242-248 ℃
FT-IR (KBr, cm ^-1 ): 1564 (w), 1385 (w), 1292 (s), 1088 (m), 814 (s), 802 (s), 687 (s), 590 (w) .
¹ H NMR (300 MHz, 25 oC, CDCl ₃ ): 7.56 (dd, J = 12.9, 5.4Hz 4H), 8.06 (d, J = 9.0 Hz, 2H), 8.23 (s, 2H), 8.69 (d, J = 9.0 Hz, 2H).
¹³ C [ ¹ H] NMR (150 MHz, 25 oC, CDCl ₃ ): 120.4, 122.7, 123.7, 125.1, 125.8, 127.1, 127.7, 137.8, 138.9.
MS (EI, m / z (relative intensity)): 290 (M +, 98), 289 (36), 258 (59), 243 (28), 209 (20), 207 (21), 145 (100), 127 (25), 99 (22), 82 (21).
Anal. Calcd for C ₁₈ H ₁₀ S ₂ : C, 74.45; H, 3.47%. Found: C, 74.52; H, 3.47%.

  The obtained compound 8, compound 16, compound 19, compound no. It was confirmed that the compound No. 22, compound 25, compound 28 and compound 31 can be produced in the same manner as in the known method and show the same performance.

Claims (10)

A compound represented by the following general formula (1) by coupling the compound (b) represented by the following general formula (2) and the compound (c) represented by the following general formula (3). Step 1 for producing (a);
And a process 2 for dehydrohalogenating the compound (a) represented by the following general formula (1), and a method for producing a picene represented by the following general formula (4) and a derivative thereof.

(In the formula, X ₁ and X _{2 each} represent a halogen atom, and R ₇ and R ₈ each independently represent a hydrogen atom, a halogen atom, a nitro group, a hydroxyl group, an alkylcarbonyloxy group having 1 to 20 carbon atoms, or 1 to 1 carbon atoms. 20 substituent amino group which may have a carboxyl group, a carboxyl group forming salts with bases, Luke carboxyl group to form an ester with an alcohol having 1 to 20 carbon atoms, have a substituent Indication of hydrocarbon groups having 1 to 20 carbon atoms which may have a group represented by an alkoxy group or a -SiR ₁₃ R ₁₄ R ₁₅ having 1 to 20 carbon atoms that may have a substituent, R ₁₃ R ₁₄ and R ₁₅ each independently represent a hydrogen atom or a hydrocarbon group having 1 to 20 carbon atoms which may have a substituent.

(In the formula, Ar represents an aryl group, and the hydrogen atom in Ar has a halogen atom, a nitro group, a hydroxyl group, an alkylcarbonyloxy group having 1 to 20 carbon atoms, and a substituent having 1 to 20 carbon atoms. an amino group which may be a carboxyl group, a carboxyl group forming salts with bases, alcohols and esters formed have Luke carboxyl group having 1 to 20 carbon atoms, carbon atoms which may have a substituent 1 _May be substituted with a hydrocarbon group having ˜20, an alkoxy group having 1 to 20 carbon atoms which may have a substituent, or —SiR ₁₃ R ₁₄ R ₁₅ , and R ₅ and R ₆ are each independently hydrogen. Forms a salt with an atom, a halogen atom, a nitro group, a hydroxyl group, an alkylcarbonyloxy group having 1 to 20 carbon atoms, an amino group that may have a substituent having 1 to 20 carbon atoms, a carboxyl group, or a base Carboxy Group, to form an ester with an alcohol having 1 to 20 carbon atoms Luke carboxyl group, optionally substituted hydrocarbon group having 1 to 20 carbon atoms carbon atoms, which may have a substituent 1 to 20 alkoxy groups or a group represented by —SiR ₁₃ R ₁₄ R ₁₅ , R ₁₁ and R ₁₂ each independently represent a hydrogen atom or an alkoxy group having 1 to 20 carbon atoms, and R ₁₁ and R ₁₂ May form a ring, and R ₁₃ , R ₁₄ and R ₁₅ each independently represent a hydrogen atom or a hydrocarbon group having 1 to 20 carbon atoms which may have a substituent.

(Wherein X ₁ represents a halogen atom, Ar, R ₅ and R ₆ are the same as in the above general formula (3), R ₇ and R ₈ are the same as in the above general formula (2), Ar, R ₅ or R ₆ may be different from each other, and the hydrogen atom in Ar may be substituted in the same manner as in the general formula (3).

(In the formula, Ar, R ₅ and R ₆ are the same as in the general formula (3), two Ar, R ₅ or R ₆ may be different from each other, and the hydrogen atom in Ar is (It may be substituted in the same manner as in formula (3).)   The method for producing picene and derivatives thereof according to claim 1, wherein the reaction in step 1 is carried out in the presence of a catalyst comprising a transition metal compound and a tri-substituted phosphine and a base.   The transition metal compound used in step 1 is at least one selected from the group consisting of palladium compounds, rhodium compounds, platinum compounds, nickel compounds, cobalt compounds, copper compounds, iron compounds, iridium compounds, ruthenium compounds, silver compounds and gold compounds. The method for producing picene and derivatives thereof according to claim 2, which is a kind of transition metal compound.   The method for producing picene and derivatives thereof according to claim 2 or 3, wherein the trisubstituted phosphine used in step 1 is at least one trisubstituted phosphine selected from the group consisting of trialkylphosphine and triarylphosphine.   The method for producing picene and derivatives thereof according to any one of claims 2 to 4, wherein the base used in step 1 is potassium hydroxide or sodium hydroxide.   The method for producing picene and derivatives thereof according to claim 1 or 2, wherein the reaction in step 2 is carried out in the presence of a catalyst comprising a transition metal compound and a tri-substituted phosphine and a base.   The transition metal compound used in step 2 is at least one selected from the group consisting of palladium compounds, rhodium compounds, platinum compounds, nickel compounds, cobalt compounds, copper compounds, iron compounds, iridium compounds, ruthenium compounds, silver compounds and gold compounds. The method for producing picene and derivatives thereof according to claim 6, which is a kind of transition metal compound.   The trisubstituted phosphine used in step 2 is at least one trisubstituted phosphine selected from the group consisting of tricycloalkylphosphine, trialkylphosphine and triarylphosphine. Production method.   The method for producing picene and derivatives thereof according to any one of claims 6 to 8, wherein the base used in step 2 is an alkali metal carbonate. A compound represented by the following general formula (1).

(Wherein X ₁ represents a halogen atom, Ar, R ₅ and R ₆ are the same as in the above general formula (3), R ₇ and R ₈ are the same as in the above general formula (2), Ar, R ₅ or R ₆ may be different from each other, and the hydrogen atom in Ar may be substituted in the same manner as in the general formula (3).