JP2011111412A - Method for manufacturing cyclic aliphatic diamine having trans-structure - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide a method for manufacturing a cyclic aliphatic diamine having a trans-structure expected to be useful as a monomer for a polyurethane resin or a polyamide resin or a raw material thereof, or as an intermediate for raw materials of pharmaceuticals and agrochemicals. <P>SOLUTION: The method for manufacturing the cyclic aliphatic diamine having a trans-structure represented by general formula (2) comprises imidizing a dihalide compound consisting of a trans-structure and a cis-structure by means of an imide compound followed by a decomposition reaction, where 1-5 mole, based on 1 mole of the dihalide compound having a cis-structure, of a basic compound is used on imidization. In the formula, the dotted line represents a single bond or a double bond. <P>COPYRIGHT: (C)2011,JPO&INPIT

Description

  The present invention relates to a novel method for producing a cycloaliphatic diamine having a trans isomer structure, and is expected to be useful as an intermediate for polyurethane resin and polyamide resin monomers, raw materials, and pharmaceutical and agrochemical raw materials. The present invention provides a novel process for producing a cycloaliphatic diamine having a trans isomer structure.

  In recent years, a polyurethane resin using a cyclic aliphatic diisocyanate having an aliphatic hydrocarbon having a cyclic structure as a raw material has no yellowing, weather resistance, and rigidity, and has attracted attention as a paint or an adhesive. Since the three-dimensional structure of the isocyanate group of the cycloaliphatic diisocyanate affects the physical properties of the polyurethane resin, it is expected to have a trans structure. In general, since the steric structure of the diisocyanate group retains the stericity of the amino group of the diamine used as a raw material, the cycloaliphatic diamine used as the raw material of the cyclic aliphatic diisocyanate is desired to have a trans isomer structure. Yes.

  For example, trans-1,2-bis (aminomethyl) -cyclohexane is known as a cycloaliphatic diamine having such a trans structure, and the production method thereof is to hydrogenate the nitrile group of phthalonitrile. Has proposed a method for producing o-xylylenediamine by further hydrogenating this o-xylylenediamine (see, for example, Patent Document 1).

  In addition, a method for selectively producing a trans isomer by isomerizing a cis isomer and converting it to a trans isomer has been proposed (see, for example, Patent Document 2).

Japanese Patent Laid-Open No. 06-279368 (Claims) JP-A-10-259167 (Claims)

  However, in the method proposed in Patent Document 1, 1,2-bis (aminomethyl) -cyclohexane produced by nuclear hydrogenation is a mixture of cis-trans structural isomers, so that only the trans isomer is selectively obtained. There was a problem that it was not possible.

  Moreover, in the method proposed in Patent Document 2, it is necessary to use expensive phthalonitrile, the harsh reaction conditions are necessary for the nuclear hydrogenation of the aromatic ring, and the complicated process of undergoing isomerization. There were problems such as becoming a process.

  Therefore, the present invention has been made in view of the above problems, and its purpose is to use a readily available raw material mixed with a trans isomer and a cis isomer, without a complicated and special process, It is an object of the present invention to provide a novel production method for selectively producing a cycloaliphatic diamine having a trans isomer structure, which is expected to be useful as an intermediate for polyamide resin monomers, raw materials, and raw materials for medicines and agricultural chemicals.

  As a result of intensive studies to solve the above-mentioned problems, the present inventors have found a novel method for producing a cycloaliphatic diamine having a trans isomer structure and have completed the present invention.

  That is, the present invention provides a trans isomer represented by the following general formula (2), in which a dihalide having a trans isomer structure and a cis isomer structure represented by the following general formula (1) is imidized with an imide compound and then decomposed. A method for producing a cycloaliphatic diamine having a structure, wherein 1 to 5 mol of a basic compound is used per 1 mol of a dihalide having a cis structure at the time of imidation. The present invention relates to a process for producing a cycloaliphatic diamine having a trans isomer structure.

（式中、点線は単結合又は二重結合を示し、Ｘはそれぞれ独立して塩素原子、臭素原子又はヨウ素原子を表す。）

(In the formula, a dotted line represents a single bond or a double bond, and each X independently represents a chlorine atom, a bromine atom or an iodine atom.)

（式中、点線は単結合又は二重結合を表す。）
以下、本発明について詳細に説明する。

(In the formula, the dotted line represents a single bond or a double bond.)
Hereinafter, the present invention will be described in detail.

  The present invention relates to a novel process for producing a cycloaliphatic diamine having a trans isomer structure represented by the general formula (2), and comprises a trans isomer structure and a cis isomer structure represented by the general formula (1). When the dihalide is imidized with an imide compound, 1 mol of a basic compound is used for 1 mol of a dihalide having a cis structure, and then a decomposition reaction is performed. It is a manufacturing method of cycloaliphatic diamine.

  Examples of the cycloaliphatic diamine having the trans isomer structure produced by the production method of the present invention include trans-1,2-bis (aminomethyl) -cyclohexane, trans-1,2-bis (aminomethyl) -4. -Cyclohexene is mentioned, and among them, trans-1,2-bis (aminomethyl) -cyclohexane is preferable since the cyclic aliphatic diamine itself has high stability.

  Examples of the dihalide having a trans isomer structure and a cis isomer structure represented by the general formula (1) used in the production method of the present invention include 1,2-bis (chloromethyl) -cyclohexane, 1,2-bis. (Bromomethyl) -cyclohexane, 1,2-bis (iodomethyl) -cyclohexane, 1,2-bis (chloromethyl) -4-cyclohexene, 1,2-bis (bromomethyl) -4-cyclohexene, 1,2-bis ( Examples thereof include dihalides having a trans isomer structure and a cis isomer structure such as iodomethyl) -4-cyclohexene. Among these, since raw materials are easily available and can be produced simply and efficiently, 1,2-bis (chloromethyl) -cyclohexane, wherein X in the general formula (1) are both chlorine atoms, 1,2 A dihalide composed of a trans-form structure and a cis-form structure of bis (chloromethyl) -4-cyclohexene is preferable, and since the stability is particularly high, the trans-form structure and cis of 1,2-bis (chloromethyl) -cyclohexane More preferred are dihalides having a body structure.

  The dihalide having a trans isomer structure and a cis isomer structure represented by the general formula (1) used in the production method of the present invention is a dihalide having a trans isomer structure represented by the following general formula (3). And a mixture of dihalides having a cis structure represented by the following general formula (4).

（式中、点線は単結合又は二重結合を示し、Ｘ_１はそれぞれ独立して塩素原子、臭素原子又はヨウ素原子を表す。）

(In the formula, a dotted line represents a single bond or a double bond, and X ₁ each independently represents a chlorine atom, a bromine atom or an iodine atom.)

（式中、点線は単結合又は二重結合を示し、Ｘ_２はそれぞれ独立して塩素原子、臭素原子又はヨウ素原子を表す。）
ここで、上記一般式（３）で表されるトランス体構造を有するジハロゲン化物としては、例えばトランス−１，２−ビス（クロロメチル）−シクロヘキサン、トランス−１，２−ビス（ブロモメチル）−シクロヘキサン、トランス−１，２−ビス（ヨードメチル）−シクロヘキサン、トランス−１，２−ビス（クロロメチル）−４−シクロヘキセン、トランス−１，２−ビス（ブロモメチル）−４−シクロヘキセン、トランス−１，２−ビス（ヨードメチル）−４−シクロヘキセン等があげられる。ここで、上記一般式（３）で表されるトランス体構造を有するジハロゲン化物のハロゲン化メチル基、例えばクロロメチル基は互いに環構造が作る面の反対側に位置している。これらのうち、原料入手が容易で、簡便に効率よく製造できることから、上記一般式（３）におけるＸ_１がともに塩素原子であるトランス−１，２−ビス（クロロメチル）−シクロヘキサン、トランス−１，２−ビス（クロロメチル）−４−シクロヘキセンが好ましく、特に安定性が高いことから、トランス−１，２−ビス（クロロメチル）−シクロヘキサンがさらに好ましい。

(In the formula, a dotted line represents a single bond or a double bond, and X ₂ each independently represents a chlorine atom, a bromine atom or an iodine atom.)
Here, examples of the dihalide having a trans isomer structure represented by the general formula (3) include trans-1,2-bis (chloromethyl) -cyclohexane and trans-1,2-bis (bromomethyl) -cyclohexane. , Trans-1,2-bis (iodomethyl) -cyclohexane, trans-1,2-bis (chloromethyl) -4-cyclohexene, trans-1,2-bis (bromomethyl) -4-cyclohexene, trans-1,2 -Bis (iodomethyl) -4-cyclohexene and the like. Here, the methyl halide group of the dihalide having the trans isomer structure represented by the general formula (3), such as a chloromethyl group, is located on the opposite side of the plane formed by the ring structure. Among these, since raw materials are easily available and can be easily and efficiently produced, trans-1,2-bis (chloromethyl) -cyclohexane, trans-1 in which X ₁ in the general formula (3) is a chlorine atom. , 2-bis (chloromethyl) -4-cyclohexene is preferred, and trans-1,2-bis (chloromethyl) -cyclohexane is more preferred because of its particularly high stability.

Examples of the dihalide having a cis structure represented by the general formula (4) include cis-1,2-bis (chloromethyl) -cyclohexane, cis-1,2-bis (bromomethyl) -cyclohexane, Cis-1,2-bis (iodomethyl) -cyclohexane, cis-1,2-bis (chloromethyl) -4-cyclohexene, cis-1,2-bis (bromomethyl) -4-cyclohexene, cis-1,2- Bis (iodomethyl) -4-cyclohexene and the like can be mentioned. Here, the methyl halide group of the dihalide having the cis structure represented by the general formula (4), for example, the chloromethyl group, is located on the same side of the surface formed by the ring structure. Among these, cis-1,2-bis (chloromethyl) -cyclohexane, cis-, in which X ₂ in the general formula (4) is both a chlorine atom because raw materials are easily available and can be produced easily and efficiently. 1,2-bis (chloromethyl) -4-cyclohexene is preferred, and cis-1,2-bis (chloromethyl) -cyclohexane is more preferred because of particularly high stability.

  The ratio of the dihalide having a trans isomer structure to the dihalide having a cis isomer structure in the mixture used in the production method of the present invention is not limited, and among them, a cycloaliphatic diamine having a trans isomer structure can be produced in a high yield. Therefore, 99: 1 to 30:70 is preferable, and 99: 1 to 50:50 is particularly preferable.

  In the production method of the present invention, when the dihalide composed of the trans isomer structure and the cis isomer structure represented by the general formula (1) is imidized with an imide compound, 1 mol of the dihalide having the cis isomer structure is used. The imidization is performed using 1 to 5 mol of the basic compound.

  The imide compound is not particularly limited. For example, sodium phthalimide, potassium phthalimide, phthalimide cesium, sodium tetrachlorophthalimide, potassium tetrachlorophthalimide, tetrachlorophthalimide cesium, nitrophthalimide sodium, nitrophthalimide potassium, nitrophthalimide cesium, aminophthalimide sodium Aminophthalimide potassium, Aminophthalimide cesium, Sodium bromophthalimide, Bromophthalimide potassium, Bromophthalimide cesium, Naphthalimide sodium, Naphthalimide potassium, Naphthalimide cesium, Ethosuccimide sodium, Ethosuximide potassium, Ethosuximide cesium, Succinic acid Sodium imido, succinimide potassium Cesium imidocesium succinate, maleimide sodium, maleimide potassium, maleimide cesium, glutarimide sodium, glutarimide potassium, glutarimide cesium, dimethyl glutarimide sodium, dimethyl glutarimide potassium, dimethyl glutarimide cesium, tetramethylene glutarimide sodium, tetra Examples include methylene glutarimide potassium and tetramethylene glutarimide cesium.

  There is no restriction on the amount of the imide compound used at the time of imidization. Among them, the amount of expensive imide compound used can be suppressed, and the amount of waste derived from the imide compound can be suppressed and the imidization can proceed efficiently. Therefore, it is preferable that it is 2-5 mol of imide compounds with respect to 1 mol of dihalides which have a trans body structure, and it is especially preferable that it is 2-3 mol.

  Moreover, in the manufacturing method of this invention, 1-5 mol of basic compounds are used with respect to 1 mol of dihalides which have a cis body structure at the time of this imidation. By using the basic compound, a dihalide having a cis structure is selectively dehalogenated and removed from the reaction system as a side reaction product. Therefore, a cycloaliphatic diamine having a trans isomer structure is selectively produced. When the basic compound is less than 1 mol, the imide compound is consumed by the dihalide having a cis structure, and thus imidation of the dihalide having a trans isomer structure does not proceed well, and the cycloaliphatic having a trans isomer structure It becomes difficult to produce diamine efficiently. On the other hand, when the basic compound exceeds 5 mol, the dihalide having a trans isomer structure also undergoes a dehalogenation reaction, making it difficult to efficiently produce a cycloaliphatic diamine having a trans isomer structure. And since the cycloaliphatic diamine which has a trans body structure is obtained more selectively, and also the usage-amount of an imide compound can be suppressed more, basic compound 1.5 ~ with respect to 1 mol of dihalides which have a cis body structure. It is preferable to set it as 5 mol, and it is preferable to set it as 2-4 mol especially.

  The basic compound is not particularly limited, and examples thereof include alkali metal hydroxides such as lithium hydroxide, sodium hydroxide, potassium hydroxide, and cesium hydroxide; alkali metal carbonates such as sodium carbonate and potassium carbonate; sodium Alkali metal alkoxides such as methoxide, sodium ethoxide, potassium methoxide, potassium ethoxide, lithium-t-butoxide, sodium-t-butoxide, potassium-t-butoxide; lithium hydride, sodium hydride, potassium hydride And alkali metal hydrides such as methyl lithium and butyl lithium; alkali metal amides such as lithium amide and sodium amide; organic bases such as pyridine, lutidine and toluidine. These basic compounds can be used alone or in combination of two or more. Among these, since a cycloaliphatic diamine having a trans isomer structure is obtained more selectively, it may be an alkali metal hydroxide such as lithium hydroxide, sodium hydroxide, potassium hydroxide, cesium hydroxide, etc. Sodium hydroxide is particularly preferable.

  The imidization can also be carried out in a solvent. Examples of the solvent used here include water; n-pentane, n-hexane, n-heptane, n-octane, n-nonane, n-decane and the like. Aliphatic hydrocarbons; Cyclopentane, cyclohexane, methylcyclohexane, dimethylcyclohexane, cyclooctane, decahydronaphthalene and other alicyclic hydrocarbons; benzene, toluene, xylene and other aromatic hydrocarbons; ethyl ether, tetrahydrofuran, Ethers such as dioxane, diglyme and triglyme; alcohols such as methanol, ethanol, n-propanol, isopropanol, n-butanol, isobutanol, sec-butanol and tert-butanol; ketones such as acetone and methyl ethyl ketone; N-methylpyrrolide , Dimethylformamide, amides such as dimethylacetamide; dimethylsulfoxide; dichloromethane, chloroform, carbon tetrachloride, dichloroethane, trichloroethane, halogenated hydrocarbons such as tetrachloroethane and the like. These solvents can be used alone or in combination of two or more. And since imidation reaction advances easily, amides, such as N-methylpyrrolidone, dimethylformamide, dimethylacetamide, are preferable, and dimethylformamide is especially preferable.

  There is no restriction | limiting in the reaction temperature in the case of imidation, For example, it is -50-300 degreeC, Preferably it is 0-200 degreeC. There is no restriction | limiting also in reaction pressure, Usually, it is 0.001-30 MPa by an absolute pressure, Preferably it is 0.1-15 MPa. The reaction time may be appropriately selected depending on the temperature and the substrate concentration of the raw material, and is usually 1 second to 100 hours. There is no limitation on the atmosphere during the imidation reaction, and it is desirable to perform the reaction while avoiding air. For example, the imidization reaction is preferably performed in an inert gas atmosphere such as nitrogen, argon, or helium.

  The imidization method is not limited, and is a dihalide having a trans isomer structure and a cis isomer structure represented by the above general formula (1) as a raw material, and further a trans isomer represented by the above general formula (3). A mixture of a dihalide having a structure and a dihalide having a cis-form structure represented by the general formula (4), a batch system for charging an imide compound, a basic compound and a solvent into a reaction apparatus, the mixture as a raw material, and an imide compound In addition, the basic compound, the solvent, and the like can be continuously supplied and the unreacted raw material and the reaction solution can be continuously extracted. In addition, the raw material charging order is not particularly limited, the raw material mixture, the imide compound, the basic compound and the solvent are mixed at once, and the raw material mixture, the basic compound and the solvent are contacted in advance. And a method of mixing with an imide compound. Among these, since the use amount of the imide compound can be suppressed, a method in which the mixture, which is a raw material, a basic compound, and if necessary, a solvent is contacted in advance and then mixed with the imide compound is preferable.

  After completion of the reaction, the product can be separated by a known separation method. For example, the product can be separated by distillation or precipitation from a solvent and filtration.

  In the production method of the present invention, the product imidized with the imide compound is then subjected to a decomposition reaction, whereby a cycloaliphatic diamine having a trans isomer structure represented by the general formula (2) is produced. . There is no restriction | limiting in particular as a reactive agent used by this decomposition reaction, For example, an acid, a base, or hydrazine etc. are mentioned.

  Examples of the acid include inorganic acids such as hydrochloric acid, nitric acid and sulfuric acid; carboxylic acids such as formic acid, acetic acid, propionic acid and oxalic acid; phenol and the like. Examples of the base include lithium hydroxide, sodium hydroxide, potassium hydroxide, rubidium hydroxide, cesium hydroxide, magnesium hydroxide, calcium hydroxide, strontium hydroxide, barium hydroxide, lithium carbonate, sodium carbonate, potassium carbonate, Rubidium carbonate, cesium carbonate, magnesium carbonate, calcium carbonate, strontium carbonate, barium carbonate, lithium bicarbonate, sodium bicarbonate, potassium bicarbonate, rubidium bicarbonate, cesium bicarbonate, magnesium bicarbonate, calcium bicarbonate, strontium bicarbonate, And inorganic bases such as barium bicarbonate. Examples of hydrazines include hydrazine, methyl hydrazine, ethyl hydrazine, propyl hydrazine, phenyl hydrazine, o-tolyl hydrazine, m-tolyl hydrazine, p-tolyl hydrazine and the like. Among these, since the decomposition reaction is easy and the cycloaliphatic diamine represented by the general formula (2) can be produced with good yield, lithium hydroxide, sodium hydroxide, potassium hydroxide, water Preferred are inorganic bases such as rubidium oxide and cesium hydroxide, or hydrazines such as hydrazine, methyl hydrazine, ethyl hydrazine, propyl hydrazine, phenyl hydrazine, o-tolyl hydrazine, m-tolyl hydrazine, p-tolyl hydrazine, and particularly hydrazine is preferred. .

  And there is no restriction | limiting in the preparation ratio of the imidation product and the reagent used by decomposition | disassembly reaction, Among them, since decomposition | disassembly reaction advances efficiently, 1 mol of dihalides represented by the said General formula (1) is mentioned. The reaction agent is preferably used in an amount of 2 to 100 mol, particularly preferably 2 to 50 mol, and more preferably 2 to 20 mol.

  In addition, the decomposition reaction with the reactant can also be performed in a solvent, and examples of the solvent include water; n-pentane, n-hexane, n-heptane, n-octane, n-nonane, n -Aliphatic hydrocarbons such as decane; Alicyclic hydrocarbons such as cyclopentane, cyclohexane, methylcyclohexane, dimethylcyclohexane, cyclooctane, decahydronaphthalene; Aromatic hydrocarbons such as benzene, toluene, xylene; Ethyl Ethers such as ether, tetrahydrofuran, dioxane, diglyme and triglyme; alcohols such as methanol, ethanol, n-propanol, isopropanol, n-butanol, isobutanol, sec-butanol and tert-butanol; ketones such as acetone and methyl ethyl ketone N-methyl Pyrrolidone, dimethyl formamide, amides such as dimethylacetamide; dimethylsulfoxide; dichloromethane, chloroform, carbon tetrachloride, dichloroethane, trichloroethane, halogenated hydrocarbons such as tetrachloroethane and the like. These solvents can be used alone or in combination of two or more. And since the decomposition reaction is likely to proceed, water; alcohols such as methanol, ethanol, n-propanol, isopropanol, n-butanol, isobutanol, sec-butanol, tert-butanol; N-methylpyrrolidone, dimethylformamide An amide such as dimethylacetamide is preferable, and methanol, ethanol, and dimethylformamide are particularly preferable.

  There is no restriction | limiting in the reaction temperature in this decomposition reaction, For example, it is -50-200 degreeC, Preferably it is 0-150 degreeC. There is no restriction | limiting also in reaction pressure, Usually, it is 0.1-30 Mpa in absolute pressure, Preferably it is 0.1-10 Mpa. The reaction time may be appropriately selected depending on the temperature and the substrate concentration of the raw material, and is usually 1 minute to 100 hours. The atmosphere during the decomposition reaction is not limited, and it is desirable to avoid air, and it is preferable to carry out the reaction in an inert gas atmosphere such as nitrogen, argon or helium.

  There is no limitation on the method for the decomposition reaction. Any of the reaction raw material and the continuous type in which the reaction solution is continuously extracted can be used. Moreover, there is no restriction | limiting also in a reaction state, It can carry out in a liquid phase or a solid-liquid mixed state.

  And in the manufacturing method of this invention, the cycloaliphatic diamine which has the trans body structure represented by the said General formula (2) manufactured by the method of well-known separation methods, for example, distillation etc., is recoverable.

  A dihalide having a trans isomer structure and a cis isomer structure represented by the general formula (1) used in the production method of the present invention, particularly a dihalide having a trans isomer structure represented by the general formula (3) and the above general formula. The mixture of dihalides having a cis isomer structure represented by the formula (4) may be produced by any method. For example, 1,3-butadiene is represented by 1,4-butadiene represented by the following general formula (5). By reacting with dihalogeno-2-butene, it can be efficiently produced as a dihalide having a double bond. Further, by dihydrating a dihalide having a double bond with hydrogen, it is possible to produce a dihalide whose ring structure is entirely composed of single bonds.

（式中、Ｙはそれぞれ独立して塩素原子、臭素原子又はヨウ素原子を表す。）
ここで、トランス体構造を有するジハロゲン化物とシス体構造を有するジハロゲン化物の比を高めるためには、原料として用いる１，４−ジハロゲノ−２−ブテンの立体構造が重要で、トランス体がシス体よりも比率の高い１，４−ジハロゲノ−２−ブテンを用いることが好ましい。

(In formula, Y represents a chlorine atom, a bromine atom, or an iodine atom each independently.)
Here, in order to increase the ratio of the dihalide having a trans isomer structure to the dihalide having a cis isomer structure, the three-dimensional structure of 1,4-dihalogeno-2-butene used as a raw material is important, and the trans isomer is a cis isomer. It is preferable to use 1,4-dihalogeno-2-butene having a higher ratio.

  The cycloaliphatic diamine having a trans structure produced according to the present invention is expected to be useful as a polyurethane resin or polyamide resin monomer, its raw material, and an intermediate for raw materials for medicines and agricultural chemicals.

  The cycloaliphatic diamine having a trans isomer structure obtained by the production method of the present invention is expected to be useful as an intermediate for polyurethane and polyamide resin monomers, raw materials, and pharmaceutical and agrochemical raw materials. The production method is expected to be very useful industrially.

  Examples of the present invention are shown below, but the present invention is not limited to these examples.

  The measurement methods used in the examples are shown below.

<Gas chromatographic analysis>
N-methylpyrrolidone was added to the reaction solution as an internal standard, and a gas chromatograph (manufactured by Shimadzu Corporation, manufactured by GL Sciences (trade name) TC-1) and equipped with an FID detector (hydrogenated flame ionization detector) ( (Product name) GC-1700) was injected with 0.4 μl of the reaction solution, and analysis was performed under the conditions of a vaporization chamber temperature of 250 ° C. and a detector temperature of 320 ° C.

<GC-MS measurement>
Using a gas chromatograph mass spectrometer (GC part; manufactured by Hewlett-Packard, (trade name) HP6890, MS part; manufactured by JEOL, (trade name) JMS-700), a vaporization chamber temperature of 250 ° C. and a detector temperature of 320 ° C. Measurement was performed under the conditions.

Synthesis example 1
(Synthesis of cycloaliphatic dihalides having double bonds in the ring)
150 g (1.2 mol) of 1,4-dichloro-2-butene (trans isomer: cis isomer = 90: 10) was charged into a 500 ml autoclave. After the inside was replaced with nitrogen, the temperature was raised to 180 ° C. with stirring, and 39.6 g (0.733 mol) of 1,3-butadiene was supplied by a pump over 8 hours and 30 minutes. After completion of the supply, the mixture was further heated and stirred for 6 hours to carry out Diels-Alder reaction. After completion of the reaction, the temperature was lowered to 25 ° C., and the reaction solution was taken out from the autoclave. The reaction solution was a brown solution. The resulting brown solution was distilled under a reduced pressure of 0.4 kPa and the distillate in the range of 65 to 75 ° C. was collected to obtain 1,2-bis (chloromethyl) -4-cyclohexene having a purity of 90% by weight. 14 g (yield based on 1,3-butadiene: 10%) was obtained as a colorless solution.
(Synthesis of cycloaliphatic dihalides whose ring structures are all single bonds)
Into a 300 ml autoclave is placed 10 g of 1,2-bis (chloromethyl) -4-cyclohexene obtained above, 100 g of ethanol and 0.1 g of 5 wt% Pd / C (manufactured by N.E. Chemcat) as a hydrogenation catalyst. And replaced with nitrogen. Thereafter, the temperature in the autoclave was raised to 50 ° C. while stirring, hydrogen was supplied and maintained at 1.0 MPa, and the reaction solution was taken out after 2 hours. The obtained reaction solution was filtered and distilled under a reduced pressure of 0.4 kPa, and the distillate in the range of 70 to 79 ° C. was collected and analyzed by gas chromatography. As a result, 1,2-bis (chloromethyl) -4-cyclohexene was obtained. Was completely converted to obtain 1,2-bis (chloromethyl) -cyclohexane (trans isomer: cis isomer = 81: 19) with a selectivity of 95%.

Example 1
A 200 ml glass separable flask was charged with 50 g of dimethylformamide, 16 g (89 mmol) of potassium phthalimide, and 2.7 ml of an 8N aqueous sodium hydroxide solution (22 mmol, based on 1 mol of dihalide having a cis structure): 2.3 mol. Furthermore, 10 g (55 mmol, breakdown: trans isomer 40 mmol, cis isomer 9.4 mmol, other 5.5 mol) of 1,2-bis (chloromethyl) -cyclohexane obtained in Synthesis Example 1 was added, and separable while stirring. The temperature in the flask was raised to 150 ° C. and heated and stirred for 8 hours to carry out an imidization reaction. After completion of the reaction, the mixture was cooled to room temperature, 20 g of water was added, and the mixture was stirred for 30 minutes. After stirring, the solid content was separated by suction filtration using a membrane filter.

  The solid content separated by filtration was transferred to a separable flask, 100 g of ethanol was added, and the mixture was heated and stirred at 80 ° C., and 25 g (500 mmol) of hydrazine monohydrate was added under reflux of ethanol. After performing a decomposition reaction by heating and stirring at 80 ° C. for 2 hours, the mixture was cooled to room temperature and suction filtered with a membrane filter. As a result of analyzing the filtrate by gas chromatography, 1,2-bis (chloromethyl) -cyclohexane was completely converted. As a result of measuring GC-MS of the product, it was a single component and a molecular ion peak was confirmed at m / e142. The yield of trans-1,2-bis (aminomethyl) -cyclohexane was 74%, and the yield based on the trans isomer raw material was 91%.

Example 2
Except for using 3.5 ml of 8N aqueous sodium hydroxide solution (28 mol, amount based on 1 mol of dihalide having a cis isomer structure: 3.0 mol), an imidization and decomposition reaction was performed in the same manner as in Example 1, and trans- 1,2-bis (aminomethyl) -cyclohexane was obtained. The yield of trans-1,2-bis (aminomethyl) -cyclohexane was 69%. The yield based on the trans isomer raw material was 84%. No cis isomer was observed.

Example 3
Except for using 4.1 ml of an 8N aqueous sodium hydroxide solution (33 mmol, amount based on 1 mol of a dihalide having a cis isomer structure: 3.5 mol), an imidization and decomposition reaction was performed in the same manner as in Example 1, and trans- 1,2-bis (aminomethyl) -cyclohexane was obtained. The yield of trans-1,2-bis (aminomethyl) -cyclohexane was 66%. The yield based on the trans isomer raw material was 81%. No cis isomer was observed.

Example 4
Except for using 1.4 ml of 8N aqueous sodium hydroxide solution (11 mmol, amount based on 1 mol of a dihalide having a cis-structure: 1.2 mol), imidization and decomposition were carried out in the same manner as in Example 1, and trans- 1,2-bis (aminomethyl) -cyclohexane was obtained. The yield of trans-1,2-bis (aminomethyl) -cyclohexane was 65%. The yield based on the trans isomer raw material was 80%. No cis isomer was observed.

Comparative Example 1
Except that 32 g (0.170 mol) of potassium phthalimide was used and sodium hydroxide was not used, imidization and decomposition reaction were performed in the same manner as in Example 1 to obtain trans-1,2-bis (aminomethyl) -cyclohexane. It was. The yield of trans-1,2-bis (aminomethyl) -cyclohexane was 70%. The yield based on the trans isomer raw material was 86%. No cis isomer was observed. Although a high trans yield was obtained, a large amount of potassium phthalimide was required as compared with Example 1.

Comparative Example 2
Except that no 8N sodium hydroxide aqueous solution was added, imidization and decomposition reaction were performed in the same manner as in Example 1 to obtain trans-1,2-bis (aminomethyl) -cyclohexane. The yield of trans-1,2-bis (aminomethyl) -cyclohexane was 49%. The yield based on the trans isomer raw material was 60%. No cis isomer was observed.

Synthesis example 2
(Synthesis of cyclic dihalides having double bonds in the ring)
Trans isomer: cis isomer = 95: 5 except that 1,4-dichloro-2-butene was used, a Diles-Alder reaction or the like was carried out in the same manner as in Synthesis Example 1, and 1,2-bis ( Chloromethyl) 4-cyclohexene was obtained as 14 g of a colorless solution. The obtained 1,2-bis (chloromethyl) -4-cyclohexene was trans isomer: cis isomer = 90: 10.
(Synthesis of cycloaliphatic dihalides whose ring structures are all single bonds)
Using 14 g of 1,2-bis (chloromethyl) 4-cyclohexene obtained above, a hydrogenation reaction or the like was performed in the same manner as in Synthesis Example 1. 1,2-bis (chloromethyl) 4-cyclohexene was completely converted, and the selectivity for 1,2-bis (chloromethyl) cyclohexane (trans isomer: cis isomer = 90: 10) was 96%.

Example 5
Implementation was performed except that 10 g of 1,2-bis (chloromethyl) -4-cyclohexene obtained in Synthesis Example 2 was used in place of 1,2-bis (chloromethyl) -cyclohexane obtained in Synthesis Example 1. Imidization and decomposition reaction were performed in the same manner as in Example 1 to obtain trans-1,2-bis (aminomethyl) -4-cyclohexene. The yield of trans-1,2-bis (aminomethyl) -4-cyclohexene was 81%. Note that. The yield based on the trans isomer raw material was 90%. No cis isomer was observed.

Example 6
Example 1 except that 10 g of 1,2-bis (chloromethyl) -cyclohexane obtained in Synthesis Example 2 was used instead of 1,2-bis (chloromethyl) -cyclohexane obtained in Synthesis Example 1. In the same manner as above, imidization and decomposition reaction were performed to obtain trans-1,2-bis (aminomethyl) -cyclohexane. The yield of trans-trans-1,2-bis (aminomethyl) -cyclohexane was 82%. Note that. The yield based on the trans isomer raw material was 91%. No cis isomer was observed.

Claims (7)

A cycloaliphatic having a trans isomer structure represented by the following general formula (2), wherein a dihalide having a trans isomer structure and a cis isomer structure represented by the following general formula (1) is imidized with an imide compound and then decomposed. A trans diamine structure represented by the general formula (2), characterized in that 1 to 5 mol of a basic compound is used for 1 mol of a dihalide having a cis isomer structure at the time of imidization. The manufacturing method of cycloaliphatic diamine which has.

(In the formula, a dotted line represents a single bond or a double bond, and each X independently represents a chlorine atom, a bromine atom or an iodine atom.)

(In the formula, the dotted line represents a single bond or a double bond.) The dihalide represented by the general formula (1) is a mixture of a dihalide having a trans isomer structure represented by the following general formula (3) and a dihalide having a cis isomer structure represented by the following general formula (4). The method for producing a cycloaliphatic diamine having a trans isomer structure according to claim 1.

(In the formula, a dotted line represents a single bond or a double bond, and X ₁ each independently represents a chlorine atom, a bromine atom or an iodine atom.)

(In the formula, a dotted line represents a single bond or a double bond, and X ₂ each independently represents a chlorine atom, a bromine atom or an iodine atom.) The ratio of the dihalide having a trans isomer structure to the dihalide having a cis isomer structure is 99: 1 to 30:70, The cycloaliphatic diamine having a trans isomer structure according to claim 1 or 2, Manufacturing method. The method for producing a cycloaliphatic diamine having a trans isomer structure according to claim 1 or 3, wherein X in the general formula (1) is a chlorine atom. The method for producing a cycloaliphatic diamine having a trans isomer structure according to claim 2 or 3, wherein each of X ₁ and X ₂ in the general formulas (3) and (4) is a chlorine atom. The method for producing a cycloaliphatic diamine having a trans isomer structure according to any one of claims 1 to 5, wherein the basic compound is an alkali metal hydroxide. The method for producing a cycloaliphatic diamine having a trans isomer structure according to any one of claims 1 to 6, wherein the decomposition reaction is a decomposition reaction with hydrazine.