JP2008063296A - 1,5-bis(aminohydroxybenzoyl)-2,6-dimethylnaphthalene compound - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide a new diamine containing a naphthalene ring, which can be used for producing a polyamide, a polyimide and a polybenzoxazole having excellent mechanical strength, heat resistance, processability, etc., and to provide a method for producing the same. <P>SOLUTION: The new diamine is 1,5-bis(aminohydroxybenzoyl)-2,6-dimethylnaphthalene compound. The method for producing the compound comprises reacting 2,6-dimethylnaphthalene with a hydroxy(or alkoxy)nitrobenzoic acid halide in the presence of a Friedel-Crafts catalyst to give a 1,5-bis(hydroxynitrobenzoyl)-2,6-dimethylnaphthalene compound, followed by reducing the compound. <P>COPYRIGHT: (C)2008,JPO&INPIT

Description

  The present invention relates to a 1,5-bis (aminohydroxybenzoyl) -2,6-dimethylnaphthalene compound useful as a raw material for polyamide, polyimide and polybenzoxazole.

  In aromatic polymer compounds, attempts have been made to improve the heat resistance and mechanical properties by introducing a bulky molecular structure in the main chain. For such purposes, 9,9-bis (4-aminophenyl) fluorene having the following cardo structure is known as an aromatic diamine having a bulky molecular structure. (Patent Document 1)

  As aromatic diamines having a bulky molecular structure other than the cardo structure, the following 1,5-bis (4- (4-aminophenoxy) benzoyl) -2,6-dimethylnaphthalene is known. (Patent Document 2)

  Examples of the compound having a 1,5-dibenzoyl-2,6-dimethylnaphthalene structure include 1,5-bis (4-fluorobenzoyl) -2,6-dimethylnaphthalene and 1,5-bis (4-chloro) as shown below. Benzoyl) -2,6-dimethylnaphthalene and 1,5-bis (4- (4-isopropylphenoxy) benzoyl) -2,6-dimethylnaphthalene are known, which are amino groups in the benzoyl group, and hydroxy Since it is not a diamine having a group, it cannot be a raw material for polyamide, polybenzoxazole and the like.

  Examples of the orthoaminophenol compound having a naphthalene skeleton include the following 3,6-di (1-adamantyl) -2,7-bis (4-amino-3-hydroxyphenoxy) naphthalene, 5,5′-di (1 -Adamantyl) -2,2'-bis (4-amino-3-hydroxyphenoxy) -1,1'-binaphthyl, 2,7-bis (4-amino-3-hydroxyphenoxy) naphthalene is known ( Patent Document 3).

  Further improvement of various properties is increasing with respect to polymer materials, and in order to meet the demand, a new diamine compound for forming a new resin skeleton structure is required.

Japanese Patent Laid-Open No. 5-31341 JP-A-9-316190 JP 2006-151936 A Macromolecules 27, 3447-3448 (1994) Journal of Polymer Science: Part A: Polymer Chemistry, 33, 2647-2655 (1995)

  In recent years, a new diamine compound for forming a new resin skeleton structure has been demanded from the viewpoint of imparting new characteristics and further improving various characteristics. The present invention has been made to meet such demands, and the object of the present invention is to produce polyamide, polyimide and polybenzoxazole having excellent mechanical strength, heat resistance, workability and the like. It is an object of the present invention to provide a novel diamine having a naphthalene ring and a method for producing the same.

（式中、Ａは、水素、炭素数１〜３のアルキル基、ハロゲンを表す）で表される１，５−ビス（アミノヒドロキシベンゾイル）−２，６−ジメチルナフタレン化合物を提供する。 The present invention relates to the following general formula (1)

(Wherein A represents hydrogen, an alkyl group having 1 to 3 carbon atoms, or halogen), a 1,5-bis (aminohydroxybenzoyl) -2,6-dimethylnaphthalene compound represented by the formula:

（式中、Ａは、水素、炭素数１〜３のアルキル基、ハロゲンを表し、Ｒは、水素または炭素数１〜３のアルキル基を表し、Ｘはハロゲンを表す）で表されるヒドロキシ（またはアルコキシ）ニトロ安息香酸ハライド類を反応させて、下記一般式（３） The present invention also relates to 2,6-dimethylnaphthalene and the following general formula (2):

(In the formula, A represents hydrogen, an alkyl group having 1 to 3 carbon atoms, and halogen, R represents hydrogen or an alkyl group having 1 to 3 carbon atoms, and X represents halogen). Alternatively, alkoxy) nitrobenzoic acid halides are reacted to give the following general formula (3)

（式中Ａは、前記と同じ意味を表す）で表される１，５−ビス（ヒドロキシニトロベンゾイル）−２，６−ジメチルナフタレン化合物となし、これを還元して上記の１，５−ビス（アミノヒドロキシベンゾイル）−２，６−ジメチルナフタレン化合物を製造する方法を提供する。

(In the formula, A represents the same meaning as described above) 1,5-bis (hydroxynitrobenzoyl) -2,6-dimethylnaphthalene compound represented by the above, reduced to the above 1,5-bis A method for producing a (aminohydroxybenzoyl) -2,6-dimethylnaphthalene compound is provided.

  According to the present invention, naphthalene skeleton-containing diamines useful as raw materials for polyamide, polyimide, and polybenzoxazole, and an economical production method thereof can be provided.

  The 1,5-bis (aminohydroxybenzoyl) -2,6-dimethylnaphthalene compound represented by the above general formula (1) of the present invention is a polyamide or polyimide excellent in heat resistance, mechanical properties, workability, etc. It is useful as a raw material for polybenzoxazole. In General Formula (1), A represents hydrogen; an alkyl group having 1 to 3 carbon atoms such as methyl, ethyl, isopropyl, and n-propyl; and halogen such as fluorine, chlorine, and bromine. More specifically, 1,5-bis (4-amino-3-hydroxybenzoyl) -2,6-dimethylnaphthalene, 1,5-bis (3-amino-4-hydroxybenzoyl) -2,6-dimethyl Naphthalene, 1,5-bis (2-amino-3-hydroxybenzoyl) -2,6-dimethylnaphthalene, 1,5-bis (4-amino-3-hydroxy-2-methylbenzoyl) -2,6-dimethyl Naphthalene, 1,5-bis (2-amino-3-hydroxy-4-methylbenzoyl) -2,6-dimethylnaphthalene, 1,5-bis (4-amino-2-fluoro-3-hydroxybenzoyl) -2 , 6-dimethylnaphthalene, 1,5-bis (4-amino-2-chloro-3-hydroxybenzoyl) -2,6-dimethylnaphthalene, 1,5-bis (4-amino-) - and the like can be exemplified hydroxy-2-ethyl-benzoyl) -2,6-dimethyl naphthalene. A particularly useful diamine is 1,5-bis (3-amino-4-hydroxybenzoyl) -2,6-dimethylnaphthalene.

  As shown in the following reaction formula, the 1,5-bis (aminohydroxybenzoyl) -2,6-dimethylnaphthalene compound represented by the above general formula (1) is composed of 2,6-dimethylnaphthalene and the above general formula ( 2) The nitrobenzoic acid halide represented by 2) is reacted to form the 1,5-bis (nitrobenzoyl) -2,6-dimethylnaphthalene compound represented by the general formula (3), which is reduced. Can be manufactured.

In the reaction for synthesizing a 1,5-bis (hydroxynitrobenzoyl) -2,6-dimethylnaphthalene compound by the reaction of 2,6-dimethylnaphthalene and nitrobenzoic acid halides, Friedel-Craft catalyst is used. Specific examples of nitrobenzoic acid halides used in the reaction include 3-hydroxy-4-nitrobenzoic acid chloride, 3-methoxy-4-nitrobenzoic acid chloride, 3-hydroxy-4-nitrobenzoic acid bromide, 4-hydroxy-3-nitrobenzoic acid chloride, 3-hydroxy-5-methyl-4-nitrobenzoic acid chloride, 3-fluoro-5-hydroxy-4-nitrobenzoic acid bromide, 3-ethoxy-4-nitrobenzoic acid A chloride etc. can be illustrated. Examples of Friedel-Craft catalysts that can be used in the reaction include aluminum chloride (AlCl ₃ ), iron chloride (FeCl ₃ ), tin chloride (SnCl ₄ ), titanium tetrachloride (TiCl ₄ ), and trifluoride. Examples thereof include boron (BF ₃ ).

  In the above reaction, it is also preferable to use a solvent. Examples of the solvent that can be used include nitrobenzene, dichlorobenzene, nitromethane, carbon disulfide, chloroform, 1,2-dichloroethane, and the like.

  In the said reaction, it is good to use about 1-4 mol of hydroxy (or alkoxy) nitrobenzoic acid halides with respect to 1 mol of 2,6-dimethylnaphthalene. The Friedel-Craft catalyst is preferably used in an amount of about 1 to 6 moles per mole of 2,6-dimethylnaphthalene. Furthermore, although the usage-amount of a solvent is arbitrary, it is about 1-100 mass times normally with respect to 2, 6- dimethylnaphthalene.

The reaction can be carried out in one stage, but it may be carried out in multiple stages if necessary. The reaction temperature is −10 to 200 ° C., preferably 30 to 150 ° C. The reaction time is about 1 to 100 hours, although it varies depending on the type and amount of raw materials used, the reaction temperature, and the like. When alkoxynitrobenzoic acid halides are used, the alkyl group is eliminated from the alkoxy group by this Friedel-Craft reaction and converted to a hydroxy group.
After completion of the reaction, the 1,5-bis (hydroxynitrobenzoyl) -2,6-dimethylnaphthalene compound represented by the formula (3) is recovered by appropriately combining washing with water, extraction, recrystallization, column purification, and the like. Can be purified.

  Next, a 1,5-bis (aminohydroxybenzoyl) -2,6-dimethylnaphthalene compound can be produced by reducing the 1,5-bis (hydroxynitrobenzoyl) -2,6-dimethylnaphthalene compound. it can. For the reduction, various methods such as catalytic reduction using hydrogen gas, reduction with hydrazine, reduction with a metal and an inorganic acid, reduction with a metal hydride can be employed.

  In catalytic reduction using hydrogen gas, a catalyst in which a noble metal such as palladium or platinum is supported on a support such as activated carbon, sponge nickel, or the like is used as a catalyst. These reduction catalysts are used, for example, about 0.001 to 0.5 times the mass of 1,5-bis (hydroxynitrobenzoyl) -2,6-dimethylnaphthalene compound. The reduction reaction is preferably performed in a solvent such as alcohols such as methanol and ethanol, and ethers such as tetrahydrofuran and diethyl ether. The reduction reaction can also be performed under conditions such as a hydrogen pressure of about atmospheric pressure to about 10 MPa, a reaction temperature of 0 to 100 ° C., and a reaction time of 0.1 to 100 hours.

  In the reduction with hydrazine, reduction with hydrazine and iron chloride, reduction with hydrazine and iron chloride / activated carbon, reduction with hydrazine and a noble metal catalyst, and the like can be employed. In the reduction with a metal and an inorganic acid, reduction with tin and an inorganic acid, reduction with zinc and an inorganic acid, reduction with iron and an inorganic acid, and the like can be employed. Further, in the reduction with metal hydride, a reducing agent such as lithium aluminum hydride can be used.

  After completion of the reduction reaction, the catalyst and the like are removed by filtration or the like, the reaction solvent is recovered, and the like, and then combined with extraction, recrystallization, column purification, etc. as appropriate, 1,5 represented by formula (1) -Bis (aminohydroxybenzoyl) -2,6-dimethylnaphthalene compound can be recovered or purified.

The present invention will be described in more detail with reference to the following examples, but the present invention is not limited to these examples.
(Example 1)
(1) Synthesis of 1,5-bis (4-hydroxy-3-nitrobenzoyl) -2,6-dimethylnaphthalene To 5.4 ml of 1,2-dichloroethane, 267 mg (1.71 mmol) of 2,6-dimethylnaphthalene And 415 mg (1.92 mmol) of 4-methoxy-3-nitrobenzoic acid chloride (prepared from 4-methoxy-3-nitrobenzoic acid and thionyl chloride). With stirring at room temperature or lower, 248 mg (1.86 mmol) of aluminum chloride was added. After stirring at room temperature for 2.5 hours, 413 mg (1.92 mmol) of 4-methoxy-3-nitrobenzoyl chloride and 554 mg (4.15 mmol) of aluminum chloride were added, and the mixture was further heated and refluxed for 24 hours. Chloroform was added to the reaction solution, which was washed with dilute hydrochloric acid. The separated organic layer was washed with water, washed with saturated brine, dehydrated with anhydrous magnesium sulfate and concentrated to obtain 850 mg of a tan solid. This was recrystallized from acetone to obtain 178 mg of a tan powder. (Contains 8.5% acetone)

The ¹ H-NMR spectrum of this product is shown in FIG.
¹ H-NMR (solvent CDCl ₃ ): δ (ppm) 2.29 (s, 6H), 7.25 (d, J = 9.3 Hz, 2H), 7.31 (d, J = 8.7 Hz, 2H), 7.48 (d, J = 8.7 Hz, 2H), 8.04 (brd, J = 8.1 Hz, 2H), 8.57 (brs, 2H), 10.99 (brs) , 2H)
δ (ppm) 1.61, 2.19: Peak mass spectrum derived from residual acetone (ESI−): 485 (M−H) ⁻

(2) Synthesis of 1,5-bis (3-amino-4-hydroxybenzoyl) -2,6-dimethylnaphthalene To 40 ml of methanol, 1,5-bis (4-hydroxy-3-nitrobenzoyl) -2,6 -To 1.30 g (2.67 mmol) of dimethylnaphthalene was suspended, 0.13 g of 5% palladium carbon catalyst (containing 50% water) was added, and the mixture was vigorously stirred overnight at room temperature in a hydrogen atmosphere. 40 ml of methanol and 30 ml of tetrahydrofuran were added to the reaction solution to dissolve the product, and then the palladium carbon catalyst was filtered off, and the filtrate was concentrated to obtain 1.32 g of a brown solid. A part of the solution was dissolved in an aqueous solution of triethylamine, washed with chloroform, and separated and neutralized by adding dilute hydrochloric acid to the aqueous layer obtained. The precipitate was filtered, washed with water, dried at room temperature, and then a pale yellow green solid. 490 g was obtained. To this solid, 2.3 ml of methanol was added and dissolved by heating. After cooling, crystals were precipitated, filtered and dried under reduced pressure at room temperature to obtain 400 mg of a solid. Methanol was added to a portion of the obtained solid (217 mg), heated and refluxed, cooled to room temperature, filtered, washed with methanol, and dried under reduced pressure at 50 ° C. to obtain 113 mg of a pale tan powder.

Fig. 2 shows the ¹ H-NMR spectrum, Fig. 3 shows the ¹³ C-NMR spectrum, Fig. 4 shows the infrared absorption (IR) spectrum (Nujol method), and UV-Vis absorption (UV / Vis) spectrum (solvent acetonitrile). Is shown in FIG. Moreover, the result of mass spectrum (ESI-) analysis was 425 (M-H) ^- .
¹ H-NMR (solvent CD ₃ OD): δ (ppm) 2.25 (s, 6H), 6.71 (d, J = 8.4 Hz, 2H), 7.01 (br, 2H), 7. 26 (br, s, 2H), 7.31 (d, J = 8.4 Hz, 2H), 7.45 (d, J = 8.4 Hz, 2H)
¹³ C-NMR (solvent DMSO-d ₆ ): δ (ppm) 18.95, 113.95, 120.29, 124.97, 128.30, 129.05, 129.24, 130.50, 137. 04, 137.19, 150.28, 197.57
IR spectrum: (cm ⁻¹ ) (peak numbers in parentheses), 1298 (11), 1591 (16), 1655 (17), 3307 (22), 3361 (23)
UV / Vis spectrum: (nm) (peak numbers in parentheses), 341 (1), 286 (2), 248 (3), 227.5 (4), 200.5 (5)

1 is a ¹ H-NMR spectrum of 1,5-bis (4-hydroxy-3-nitrobenzoyl) -2,6-dimethylnaphthalene obtained in Example 1. 2 is a ¹ H-NMR spectrum of 1,5-bis (3-amino-4-hydroxybenzoyl) -2,6-dimethylnaphthalene obtained in Example 1. FIG. 2 is a ¹³ C-NMR spectrum of 1,5-bis (3-amino-4-hydroxybenzoyl) -2,6-dimethylnaphthalene obtained in Example 1. FIG. 2 is an IR spectrum of 1,5-bis (3-amino-4-hydroxybenzoyl) -2,6-dimethylnaphthalene obtained in Example 1. 2 is a UV / Vis spectrum of 1,5-bis (3-amino-4-hydroxybenzoyl) -2,6-dimethylnaphthalene obtained in Example 1.

Claims (2)

The following general formula (1)

(Wherein, A represents hydrogen, an alkyl group having 1 to 3 carbon atoms, or halogen), a 1,5-bis (aminohydroxybenzoyl) -2,6-dimethylnaphthalene compound represented by: 2,6-dimethylnaphthalene and the following general formula (2)

(Wherein A represents hydrogen, an alkyl group having 1 to 3 carbon atoms, and halogen, R represents hydrogen or an alkyl group having 1 to 3 carbon atoms, and X represents a halogen). By reacting acid halides, the following general formula (3)

2. A 1,5-bis (hydroxynitrobenzoyl) -2,6-dimethylnaphthalene compound represented by the formula (wherein A represents the same meaning as described above), which is reduced. A process for producing a 1,5-bis (aminohydroxybenzoyl) -2,6-dimethylnaphthalene compound as described in 1 above.

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