JPWO2009151005A1 - Method for producing isocyanate compound - Google Patents

Abstract

Provided is a method for efficiently producing an isocyanate compound at a low reaction temperature and a low reaction pressure without using highly toxic phosgene and without going through a complicated process. An isocyanate compound is produced by reacting carbonyl fluoride with an organic amine. Carbonyl fluoride is reacted with an organic amine to produce carbamoyl fluoride, which is then converted to isocyanate. The carbamoyl fluoride is converted to isocyanate by heating.

Description

  The present invention relates to a novel method for producing an isocyanate compound.

Isocyanate compounds are the main raw materials for polyurethanes used as rigid and flexible foams, and are also widely used as raw materials for the production of elastomers, fibers and synthetic leather.
Representative isocyanate compounds produced industrially include toluene diisocyanate (TDI), diphenylmethane diisocyanate (MDI), hexamethylene diisocyanate (HDI), and the like.

These isocyanates such as TDI are mainly produced by the reaction of the corresponding organic amine and phosgene. Although the reaction of making an isocyanate by the reaction of an organic amine (RNH ₂ ) and phosgene (COCl ₂ ) is known, an isocyanate can be obtained by simply mixing and heating an organic amine and phosgene. As can be seen from the following reaction formula, a side reaction occurs in which the isocyanate reacts with the starting amine to produce urea (Non-patent Document 1).

In order to eliminate such problems, the production of urea is suppressed by converting the organic amine to hydrochloride, reacting it with phosgene to produce a carbamoyl chloride compound (RNHCOCl), and further thermally decomposing it. Thus, a method for obtaining an isocyanate compound has been proposed (Non-patent Document 2).

Currently, most of the polyisocyanate compounds such as TDI are produced industrially by applying the reaction of this organic amine hydrochloride with phosgene.
The method of synthesizing isocyanate using the reaction between organic amine hydrochloride and phosgene is as follows. (A) Amine is directly reacted with phosgene at low temperature to form a mixture of carbamoyl chloride and hydrochloride, and further reacted with phosgene at high temperature. And (b) a method of reacting with phosgene after converting the amine to hydrochloride (Patent Document 1).

The method (a) is usually carried out in two successive steps. The first stage is carried out at a low temperature in an inert solvent (for example, about 0 to 60 ° C. in the case of TDI production). The reaction between amine and phosgene produces carbamoyl chloride and hydrogen chloride at the same time. Amine hydrochloride is formed from the amine. That is, the first stage is intended to produce a mixture of carbamoyl chloride and hydrochloride. Next, in the second stage, phosgene is further reacted at a high temperature (in the case of TDI production, about 80 to 180 ° C.) to form an isocyanate (Patent Document 2). The first stage reaction is not limited to the TDI listed here, and general amines such as monoamine are also known (Non-patent Document 2).

In the method (b), in order to suppress the activity of the amine, an amine hydrochloride is synthesized in advance with an amine and hydrogen chloride and the like, and this is heated under high agitation in an inert solvent (80 ° C. to 180 ° C. for TDI production). It is made into an isocyanate by reacting with phosgene at about 0 ° C. (Patent Document 3).

  Although these methods can reduce the activity of the reaction and suppress side reactions by converting the amine to hydrochloride, it requires a step of converting the amine to its hydrochloride, and at least the second stage of dehydrochlorination There are many problems that require the salt process to be carried out at high temperature, all of which necessitates the use of highly toxic phosgene. It was desired to develop.

Various methods for producing isocyanate without using phosgene have been known so far.
For example, a reaction between an amine and dimethyl carbonate (Non-Patent Document 3), a reaction between an amine and triphosgene (Non-Patent Document 4), and a method using a nitro compound and carbon monoxide as raw materials (Patent Document 4, Non-Patent Document 5, Non-patent document 6), reaction of olefin and isocyanic acid, and decomposition of carboxylic acid azide (non-patent document 7) are known. From the standpoint of the yield of the product and the safety of the reaction, it was not suitable for industrialization.

  In addition, in the old prior art documents, in the method of obtaining isocyanate by reacting phosgene with an organic amine, carbonyl halides other than phosgene (COXY; X, Y = F, Cl, Br, I) are used. There are certainly reported examples in which isocyanate can be obtained by the same reaction as phosgene even if it is used (Patent Document 5, etc.).

  However, in this patent document, the only carbonyl halide actually used is phosgene (COXY; X, Y = Cl), and there is no demonstration using other carbonyl halides such as carbonyl fluoride. In other words, when carbonyl fluoride and organic amine are reacted, what kind of product is actually obtained, or what is its specific reaction behavior and reaction mechanism? There is no experimental support for this. Therefore, in this patent document, simply because of the similarity of conventional halogen atoms, the mere desire that all carbonyl halides such as carbonyl fluoride would exhibit similar reactivity to phosgene with respect to organic amines. It is natural to think that the synthesis reaction of isocyanate is substantially not verified from carbonyl fluoride and organic amine.

  As already seen, even though 53 years have passed since the publication of the above-mentioned Patent Document 5, the papers and patent documents relating to the process for producing isocyanates using carbonyl halides are exclusively composed of phosgene and organic compounds. It will be understood from the fact that there is nothing that is focused on carbonyl fluoride, concentrated on those utilizing reactions with amines.

Japanese Patent Laid-Open No. 2001-233853 Special Table 2006-510692 Publication British Patent No. 1146664 British Patent No. 1313199 British Patent No.727916

J. H. Saunders and R. J. Slocombe, Chem. Rev., 43, 203 (1948). W. Sieken, Liebigs Annalen der Chemie, 562, 1 (1949). Y. Wang, X.G.Zhao, F. Li, S. F. Wang and J. Zhang, J. Chem. Tech. And Biotech, 76, 857 (2001). Y. C. Charalambides and S. C. Moratti, Synthetic Commun., 37 (6), 1037 (2007). A. M. Tafesh and J. Weiguny, Chem. Rev., 96, 2035 (1996). F. Ragaini, S. Cenini, J. Mol. Catal. A: Chem. 1 (1996). S. Ozaki, Chem. Rev., 72 (5), 457 (1972).

  An object of the present invention is to provide a method for efficiently producing an isocyanate compound at a low reaction temperature and a low reaction pressure without using highly toxic phosgene and without going through a complicated process.

As a result of intensive research to achieve the above object, the inventors of the present invention can react amines with carbonyl fluoride (COF ₂ ) without using highly toxic phosgene or in the case of using phosgene. Thus, the present inventors have found that the amine can be converted into an isocyanate in a high yield without the necessity of converting the amine into a hydrochloride or passing through the amine hydrochloride in advance, thereby completing the present invention.
That is, this application provides the following inventions.
<1> A method for producing an isocyanate compound comprising reacting carbonyl fluoride with an organic amine.
<2> The method for producing an isocyanate compound according to <1>, wherein carbonyl fluoride and an organic amine are reacted to produce carbamoyl fluoride, and then the carbamoyl fluoride is converted to isocyanate.
<3> The method for producing an isocyanate compound according to <2>, wherein the carbamoyl fluoride is converted to an isocyanate by heating.
<4> The method for producing an isocyanate compound according to any one of <1> to <3>, wherein carbonyl fluoride and an organic amine are reacted and the resulting reaction mixture containing carbamoyl fluoride is subsequently heated. .
<5> The method for producing an isocyanate compound according to <4>, wherein the reaction is performed in an organic solvent.
<6> The production method according to <5>, wherein the organic solvent contains a hydrocarbon, a chlorinated hydrocarbon, or a fluorinated hydrocarbon.
<7> The method for producing an isocyanate compound according to any one of <4> to <6>, wherein the reaction is performed in a range of 80 ° C to 250 ° C.
<8> A first step of reacting carbonyl fluoride with an organic amine, excess carbonyl fluoride is removed as necessary, and the resulting reaction mixture containing carbamoyl fluoride is heated to convert it into an isocyanate compound. The manufacturing method of the isocyanate compound in any one of <1>-<3> characterized by including two processes.
<9> The process for producing an isocyanate compound according to <8>, wherein the first step is performed in an organic solvent to remove excess organic solvent and hydrogen fluoride.
<10> The method for producing an isocyanate compound according to <9>, wherein the first step is performed at less than 80 ° C.
<11> The method for producing an isocyanate compound according to <10>, wherein the reaction mixture containing carbamoyl fluoride in the second step is heated at 80 to 250 ° C.
<12> The organic amine has at least two amino (—NH ₂ ) groups, and the isocyanate compound has at least two isocyanate (—NCO) groups. Any one of <1> to <11> A process for producing the isocyanate compound according to claim 1.
<13> The isocyanate compound contains tolylene diisocyanate (TDI), diphenylmethane diisocyanate (MDI), hexamethylene diisocyanate (HDI), naphthalene diisocyanate (NDI), and tolidine diisocyanate (TODI). <12> The method for producing an isocyanate compound according to <12>.
<14> The method for producing an isocyanate compound according to <12>, wherein the organic amine is tolylenediamine (TDA) and the isocyanate compound is tolylene diisocyanate (TDI).
<15> The method for producing an isocyanate compound according to <12>, wherein the organic amine is diphenylmethanediamine (MDA) and the isocyanate compound is diphenylmethane diisocyanate (MDI).
<16> The method for producing an isocyanate compound according to <12>, wherein the organic amine is hexamethylenediamine (HDA) and the isocyanate compound is hexamethylene diisocyanate (HDI).
<17> The method for producing an isocyanate compound according to <12>, wherein the organic amine is naphthalenediamine (NDA) and the isocyanate compound is naphthalene diisocyanate (NDI).
<18> The method for producing an isocyanate compound according to <12>, wherein the organic amine is tolidine and the isocyanate compound is tolidine diisocyanate (TODI).

According to the present invention, an isocyanate compound can be efficiently produced from an amine at a low reaction temperature and a low reaction pressure without using highly toxic phosgene and without a complicated process. Incidentally, COF ₂ used in the present invention, toxic than phosgene is low _{(TLV COF2 = 2ppm, TLV COCl2} = 0.1ppm,), those more secure.

The process for producing an isocyanate compound of the present invention is characterized in that, firstly, carbonyl fluoride and an organic amine are reacted, and secondly, carbonyl fluoride and an organic amine are reacted to form a carbamoyl fluoride. And then converting the carbamoyl fluoride into an isocyanate.
The organic amine here means an organic compound having —NH ₂ group, the fluorinated carbamoyl compound (or carbamoyl fluoride) means an organic compound having —NHC (═O) F group, and an isocyanate compound. Means an organic compound having a -N = C = O group.

As mentioned earlier, some of the old prior art documents do not support any experiments, and the reaction of carbonyl halides other than phosgene with amines just because the halogen atoms are similar. There are reports that isocyanates can be obtained by similar reactions.
In this regard, the present inventors have made extensive examinations of such reports using the results and data obtained through many years of experimentation and research on fluorine compounds. In contrast, in the reaction with amine, carbonyl fluoride (COF ₂ ) and phosgene (COCl ₂ ) exhibit completely different reaction characteristics, and in the reaction between amine and phosgene, the amine is represented by the formula (3-2). It was found that carbamoyl fluoride is produced without producing amine fluoride in the reaction with carbonyl fluoride, whereas hydrochloride is by-produced. Furthermore, from this, in the production of isocyanate, it can be directly converted to isocyanate with a high yield by a simple operation step without taking measures to suppress the side reaction of reacting phosgene with an amine in advance. The new knowledge which was not known at all was acquired.

That is, as in the present invention, when COF ₂ and an amine are mixed at a low temperature, for example, unlike the above formula (3), a fluorinated carbamoyl compound (RNHCOF: R: organic amine residue) is used instead of the amine fluoride. Generate. According to the present invention, the desired isocyanate can be easily obtained by simply decomposing the carbamoyl fluoride compound.

このように、本発明によれば、COF₂を室温、有機溶媒中で、TDAなどの有機アミンと反応させてフッ化カルバモイル中間体を合成し、これを変換してTDIなどのイソシアナートを効率よく製造することができる。また、上でも述べたが、本発明で用いるCOF₂は、不燃性で、ホスゲンより毒性は低い（TLV_COF2=2ppm, TLV_COCl2=0.1ppm,)。A typical reaction found in the present invention when tolylenediamine (TDA) is used as the organic amine can be represented by the following reaction formula.

Thus, according to the present invention, COF ₂ is reacted with an organic amine such as TDA in an organic solvent at room temperature to synthesize a fluorinated carbamoyl intermediate, which is converted to efficiently convert an isocyanate such as TDI. Can be manufactured well. Although mentioned above, COF ₂ used in the present invention is a nonflammable, than low toxicity of phosgene _{(TLV COF2 = 2ppm, TLV COCl2} = 0.1ppm,).

The isocyanate synthesis method of the present invention comprises a reaction for producing carbamoyl fluoride and a reaction for obtaining isocyanate by decomposing carbamoyl fluoride, as shown in the above synthesis reaction formula.
In the present invention, these two reactions may be carried out continuously in one step (one step method), or each step may be carried out in two steps (two step method). It is more preferable to carry out by a two-stage method.

First, the isocyanate synthesis reaction according to the one-step method of the present invention will be described.
This one-step process is carried out by reacting carbonyl fluoride with an organic amine and subsequently heating the resulting reaction mixture containing carbamoyl fluoride.
The raw material organic amine used here is not particularly limited, and any of the primary organic amines used in this type of reaction can also be used. Specific examples of such amines include monoamines such as methylamine, ethylamine, propylamine, aniline, and naphthylamine, phenylenediamine, toluenediamine (TDA), methylene (diphenylamine) (MDA), and hexamethylenediamine (HAD). And diamines such as isophorone diamine (IPDA) and polyamines such as polymethylene polyphenylene polyamine (PMDA). Further, in such amine molecules, functional groups that do not interfere with the reaction, such as alkyl groups such as methyl, ethyl, and propyl groups, aryl groups such as phenyl and naphthyl groups, fluoro groups, and chloro groups. Alkoxy groups such as halogen groups, methoxy groups and ethoxy groups, aryloxy groups such as phenoxy groups and naphthoxy groups, dialkylamino groups such as dimethylamino groups and diethylamino groups, alkylthio groups such as methylthio groups and ethylthio groups, phenylthio groups and naphthylthio groups An arylthio group such as a group may be present. The amine preferably used in the present invention is a diamine such as toluenediamine (TDA), methylene (diphenylamine) (MDA), hexamethylenediamine (HAD), isophoronediamine (IPDA) or the like.

The reaction between these organic amines and COF ₂ is preferably carried out in an organic solvent with heating and stirring. In this case, the molar ratio of the amino group of the starting amine compound to COF2 is 1 to 30, preferably 2 to 20, and more preferably 2 to 10.
The heating temperature is 80 ° C to 250 ° C, preferably 130 ° C to 200 ° C, more preferably 150 ° C to 160 ° C.

  The organic solvent is not particularly limited as long as it dissolves the amine as a raw material and does not affect the reaction, but is a hydrocarbon solvent such as pentane, hexane, heptane, octane, benzene, toluene, xylene, dichloromethane, etc. Chlorinated hydrocarbon solvents such as chloroform, carbon tetrachloride, tetrachloroethylene, chlorobenzene, dichlorobenzene, 1,1,1,3,3-pentafluorobutane, 1,1,1,2,2,3,4, Fluorinated hydrocarbon solvents such as 5,5,5-decafluoropentane and 1,1,2,2,3,3,4-heptafluorocyclopentane, and ether solvents such as diethyl ether, tetrahydrofuran and dioxane Illustrated. Preferred are hydrocarbons such as dichloromethane, toluene, chlorobenzene, dichlorobenzene, 1,1,2,2,3,3,4-heptafluorocyclopentane, chlorinated hydrocarbons, and fluorinated hydrocarbons.

  In the method of the present invention, any compound that does not participate in the reaction may be mixed with the starting amine or COF2 during the reaction. Such compounds include hydrocarbons such as methane, ethane, propane, butane, benzene, toluene, xylene, halogenated hydrocarbons such as chloromethane, fluoromethane, chlorofluoromethane, chlorodifluoromethane, dimethyl ether, diethyl ether, Examples thereof include ethers such as tetrahydrofuran and dioxane.

Next, the isocyanate synthesis reaction by the two-step method of the present invention will be described.
This two-step process for synthesizing isocyanate comprises a first step of reacting carbonyl fluoride with an organic amine, and removing a surplus of carbonyl fluoride and hydrogen fluoride, and a reaction mixture containing the resulting carbamoyl fluoride. Comprising a second step of heating to convert to an isocyanate compound.

  In the first step, carbonyl fluoride and an organic amine are preferably reacted in an organic solvent. This reaction is preferably carried out with stirring. This reaction is carried out at 0 ° C to 80 ° C, preferably 10 ° C to 50 ° C, more preferably 15 ° C to 30 ° C.

In the second step, the reaction mixture containing the carbamoyl fluoride obtained in the first step is used as it is, or the remaining COF ₂ , hydrogen fluoride and / or the organic solvent is filtered, distilled at atmospheric pressure or under reduced pressure. After removing with.
It is preferably performed after removing the remaining COF ₂ , more preferably after removing the remaining COF ₂ and the organic solvent and taking out the reaction product.

The reaction for synthesizing the isocyanate in the second step is carried out by thermal decomposition or reaction with a base. Which is selected is selected by a method using hydrogen fluoride produced as a by-product.
In the case of thermal decomposition, the heating temperature is 80 ° C to 250 ° C, preferably 130 ° C to 200 ° C, more preferably 150 ° C to 160 ° C.
In the case of reaction with a base, carbonates, hydroxide salts, oxide salts, phosphate salts and fluoride salts of alkali metals or alkaline earth metals are suitable as the base, and sodium carbonate, potassium carbonate, hydroxide Examples thereof include sodium, potassium hydroxide, calcium oxide, magnesium oxide, sodium phosphate and sodium fluoride. The reaction temperature is 0 to 100 ° C., preferably at room temperature.

  In the above-described method for synthesizing isocyanate by the two-step method, the type of organic amine used as a raw material, the ratio of the organic amine and carbonyl fluoride, the type of organic solvent used, and other various configurations and conditions are as follows: What was illustrated by the 1st step method mentioned above is applied as it is.

The reaction vessel used in the present production method may be of any shape, as long as it can be used at a pressure of about 10 MPa. The material of the reaction vessel is preferably one that is not easily corroded at high temperature and high pressure in the presence of raw materials, products, HF and COF ₂ , and examples thereof include Inconel, Hastelloy, and nickel.

  Hereinafter, the present invention will be described in more detail with specific examples. However, the following specific examples are intended to illustrate the present invention, and the present invention is not limited in any way.

Example 1 Synthesis of tolylene dicarbamoyl fluoride
When 1 g of 2,4-tolylenediamine and 5 g of COF ₂ were stirred in chlorobenzene at room temperature, the product precipitated. This was filtered to obtain 1.6 g of a solid product. ¹ H-, ¹⁹ F-NMR and IR spectra of the obtained product were measured to produce 2,4-tolylene dicarbamoyl fluoride (2,4- (FCONH) ₂ C ₆ H ₃ CH ₃ ) It was confirmed.
¹ H-NMR (DMF-d ₇ , TMS): δ2.3 (s, 3H), 7.2-7.8 (m, 3H), 10.0 (br, 1H), 10.7 (br, 1H)
¹⁹ F-NMR (DMF-d ₇ , CFCl3): φ6.9 (s, 1F), 10.3 (s, 1F)
IR: 3289, 1808, 1797, 1770, 1550 cm-1

Example 2 Synthesis of diphenylmethane di (carbamoyl fluoride)
When 1 g of 4,4′-diphenylmethanediamine and 3.5 g of COF ₂ were stirred in chlorobenzene at room temperature, the product precipitated. This was filtered to obtain 1.0 g of a solid product. ¹ H-, ¹⁹ F-NMR and IR spectra of the obtained product were measured, and 4,4′-diphenylmethanedi (carbamoyl fluoride) (4,4′-FCONHC ₆ H ₄ CH ₂ C ₆ H ₄ The formation of NHCFO) was confirmed.
¹ H-NMR (CDCl ₃ , TMS): δ3.9 (s, 2H), 6.7 (br, 2H), 7.2 (m, 4H), 7.3 (m, 4H)
¹⁹ F-NMR (CDCl ₃ , CFCl3): φ6.8 (s, 1F)
IR: 3325, 1815, 1777, 1527 cm-1

Example 3 Synthesis of TDI by a one-step method
The product obtained after stirring 1 g of 2,4-tolylenediamine and 5 g of COF ₂ at 150 ° C. in chlorobenzene was analyzed by gas chromatography. From comparison with a commercially available sample, it was confirmed that 2,4-tolylene diisocyanate (2,4- (NCO) ₂ C ₆ H ₃ CH ₃ ) was produced.

Example 4 Synthesis of TDI by a two-step method
After stirring 1 g of 2,4-tolylenediamine and 5 g of COF ₂ in dichloromethane at room temperature, excess COF ₂ and the solvent were distilled off. ¹ H-, ¹⁹ F-NMR, and IR spectra of this product were measured, confirming the formation of 2,4-tolylene dicarbamoyl fluoride (2,4- (FCONH) ₂ C ₆ H ₃ CH ₃ ) (In agreement with the data of Example 1). The resulting product was heated at 180 ° C. to give 2,4-tolylene diisocyanate. As a result of analysis by ¹ H-NMR, the yield of 2,4-tolylene diisocyanate from 2,4-tolylenediamine was 92%.

Example 5 Synthesis of MDI
The reaction was conducted in the same manner as in Example 4 using 4,4′-diphenylmethanediamine instead of 2,4-tolylenediamine, and 4,4′-diphenylmethane diisocyanate (4,4′-OCNC ₆ H ₄ CH ₂ C ₆ H ₄ NCO) was obtained in 85% yield from 4,4'-diphenylmethane diamine. As in Example 4, ¹ H-, ¹⁹ F-NMR and IR spectra of the intermediate product were measured, and 4,4′-diphenylmethanedi (carbamoyl fluoride) (4,4′-FCONHC) was used as an intermediate. ₆ H ₄ CH ₂ C ₆ H ₄ NHCFO) has been confirmed.

Example 6 Synthesis of HDI After stirring 1 g of hexamethylenediamine and 2.5 g of COF ₂ in dichlorobenzene at 70 ° C., excess COF ₂ was distilled off. Next, it was heated at 180 ° C. to obtain hexamethylene diisocyanate (OCN (CH ₂ ) ₆ NCO). As a result of analysis by ¹ H-NMR, the yield of hexamethylene diisocyanate from hexamethylenediamine was 61%.

Example 7 Synthesis of NDI
The reaction was carried out in the same manner as in Example 4 using 1,5-naphthalenediamine instead of 2,4-tolylenediamine, and 1,5-naphthalene diisocyanate (1,5- (NCO) ₂ C ₁₀ H ₆ ) Was obtained in 78% yield from 1,5-naphthalenediamine.

Example 8 Synthesis of TODI
The reaction was conducted in the same manner as in Example 4 using o-tolidine instead of 2,4-tolylenediamine, and o-tolidine diisocyanate (3,3 '-(CH ₃ ) ₂ -4,4'-( NCO) ₂ (C ₆ H ₃ ) ₂ ) was obtained in 79% yield from o-tolidine.

Claims (18)

  A process for producing an isocyanate compound, comprising reacting carbonyl fluoride with an organic amine.   The method for producing an isocyanate compound according to claim 1, wherein carbamoyl fluoride is produced by reacting carbonyl fluoride with an organic amine, and then the carbamoyl fluoride is converted to isocyanate.   The method for producing an isocyanate compound according to claim 2, wherein the carbamoyl fluoride is converted to an isocyanate by heating.   The method for producing an isocyanate compound according to any one of claims 1 to 3, wherein carbonyl fluoride and an organic amine are reacted and the resulting reaction mixture containing carbamoyl fluoride is subsequently heated.   The method for producing an isocyanate compound according to claim 4, wherein the reaction is performed in an organic solvent.   The production method according to claim 5, wherein the organic solvent contains a hydrocarbon, a chlorinated hydrocarbon, or a fluorinated hydrocarbon.   The method for producing an isocyanate compound according to any one of claims 4 to 6, wherein the reaction is carried out in the range of 80 ° C to 250 ° C.   A first step of reacting carbonyl fluoride with an organic amine, and a second step of removing excess carbonyl fluoride as necessary, and heating the resulting reaction mixture containing carbamoyl fluoride to convert it to an isocyanate compound The manufacturing method of the isocyanate compound in any one of Claims 1-3 characterized by the above-mentioned.   The method for producing an isocyanate compound according to claim 8, wherein the first step is performed in an organic solvent to remove excess organic solvent and hydrogen fluoride.   The method for producing an isocyanate compound according to claim 9, wherein the first step is performed at a temperature of less than 80 ° C.   The method for producing an isocyanate compound according to claim 10, wherein the heating of the reaction mixture containing carbamoyl fluoride in the second step is performed at 80 ° C to 250 ° C. Organic amine having at least two amino (-NH ₂₎ groups, isocyanurate according to any one of claims 1 to 11 isocyanate compound is characterized by having at least two isocyanato (-NCO) group A method for producing a nate compound.   Isocyanate compounds include tolylene diisocyanate (TDI), diphenylmethane diisocyanate (MDI), hexamethylene diisocyanate (HDI), naphthalene diisocyanate (NDI), and tolidine diisocyanate (TODI). The method for producing an isocyanate compound according to claim 12.   The method for producing an isocyanate compound according to claim 12, wherein the organic amine is tolylenediamine (TDA) and the isocyanate compound is tolylene diisocyanate (TDI).   The method for producing an isocyanate compound according to claim 12, wherein the organic amine is diphenylmethanediamine (MDA) and the isocyanate compound is diphenylmethane diisocyanate (MDI).   The method for producing an isocyanate compound according to claim 12, wherein the organic amine is hexamethylenediamine (HDA) and the isocyanate compound is hexamethylene diisocyanate (HDI).   The method for producing an isocyanate compound according to claim 12, wherein the organic amine is naphthalenediamine (NDA) and the isocyanate compound is naphthalene diisocyanate (NDI).   13. The method for producing an isocyanate compound according to claim 12, wherein the organic amine is tolidine and the isocyanate compound is tolidine diisocyanate (TODI).