JP3368680B2 - Novel epoxy compound and method for producing the same - Google Patents

Description

Detailed Description of the Invention

[0001]

BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a novel epoxy compound which gives excellent cured physical properties such as heat resistance and weather resistance, a method for producing the same, and an epoxy resin cured product obtained by curing this epoxy compound.

[0002]

2. Description of the Related Art Epoxy resin is used for adhesiveness, electrical insulation,
Due to its excellent heat resistance, it can be used for electrical and electronic materials, paints,
Used in adhesives, various composite materials, civil engineering and construction materials, etc. As these epoxy resins, bisphenol A diglycidyl ether type resins are widely used.
It does not satisfy the heat resistance required for many applications. On the other hand, as the heat-resistant epoxy resin, there are phenol novolac epoxy resin and cresol novolac epoxy resin, but these have a phenyl ether bond in the structure and a main skeleton thereof is benzene, like the bisphenol A diglycidyl ether type resin. To have a ring,
There is a problem with weather resistance.

On the other hand, an epoxy compound having a structure having a triazine ring as a main skeleton, for example, a resin obtained by curing triglycidyl isocyanurate has high crystallinity, and therefore, when it is formed into a liquid compound with a liquid acid anhydride, There is a problem of crystal precipitation of triglycidyl isocyanurate.

[0004]

DISCLOSURE OF THE INVENTION The present invention provides a heat resistance which is not satisfied by a cured product obtained by curing a bisphenol A diglycidyl ether type resin, a phenol novolac epoxy resin, a cresol novolac epoxy resin, or a triglycidyl isocyanurate. Another object of the present invention is to provide a novel epoxy resin which is excellent in workability because it has excellent weatherability, does not crystallize at room temperature like triglycidyl isocyanurate, and has a low viscosity upon heating.

[0005]

Means for Solving the Problems The present invention includes the following general formula (1);

[0006]

[Chemical 4]

(Wherein R represents a hydrogen atom or a methyl group, and n represents an integer of 1 or 2). The compound of the general formula (1) is tri (carboxyalkyl) isocyanurate triglycidyl ester. In the compound of the general formula (1), when three Rs present in one molecule consist of hydrogen atoms only,
Including the case where it is composed of only a methyl group, or the case where it is composed of a combination of a hydrogen atom and a methyl group, and the three n's present in one molecule are composed of only an integer of 1 (methylene group), an integer of 2 It includes a case of being composed of only (ethylene group) or a combination of integers of 1 and 2, but it is preferable that n is composed of only an integer of 1.

The epoxy compound represented by the above general formula (1) of the present invention has the following steps a and b; a, the general formula (2);

[0009]

[Chemical 5]

(Wherein m represents an integer of 1 or 2) is added to the tri (carboxyalkyl) isocyanurate represented by the general formula (3);

[0011]

[Chemical 6]

(Wherein R ¹ represents a hydrogen atom or a methyl group, and X ¹ represents a halogen atom).
It can be manufactured by a step of adding an epihalogenohydrin to obtain an ester and a step of reacting the ester obtained in the steps b and a with an alkaline substance.

Among the tri (carboxyalkyl) isocyanurates represented by the general formula (2) used in the step a, tri (carboxymethyl) isocyanurate in which m is 1 is described in, for example, US Pat. No. 3,230,220. It is obtained by the known method described in. That is, formula (4);

[0014]

[Chemical 7]

Trisodium cyanurate represented by:
Formula (5) obtained by reacting chloracetonitrile with a solvent such as dimethylformamide at 90 ° C. for 18 hours to perform dechlorination of sodium;

[0016]

[Chemical 8]

A method in which tri (cyanomethyl) isocyanurate represented by is hydrolyzed with an acid catalyst such as hydrochloric acid. In addition, trisodium cyanuric acid of the above formula (4) and monohalogenoacetic acid ester [X ² CH ₂ COOR
² , provided that X ² is a halogen atom and R ² is an alkyl group. ] And the reaction in a solvent such as dimethylformamide, dimethylsulfoxide and the like at 80 to 120 ° C. for 5 to 20 hours to carry out dechlorination of sodium chloride to obtain the general formula (6);

[0018]

[Chemical 9]

(Wherein R ² represents an alkyl group), tri (methylcarboxylic acid alkyl) isocyanurate is treated with an acid catalyst such as hydrochloric acid or sulfuric acid, or potassium hydroxide,
There is a method of hydrolyzing with an alkali catalyst such as sodium hydroxide. Further, among the tri (carboxyalkyl) isocyanurates represented by the general formula (2) used in the above step a, tri (2-carboxyethyl) isocyanurate in which m is 2 should be obtained as a commercially available reagent. It is also possible, but the formula (7) obtained by the Michael addition reaction of acrylonitrile with cyanuric acid;

[0020]

[Chemical 10]

It can also be obtained by hydrolyzing tri (2-cyanoethyl) isocyanurate represented by the formula (3) using an acid catalyst such as hydrochloric acid or sulfuric acid. The α-epihalogenohydrin represented by the general formula (3) used in the step a of the present invention is
For example, epichlorohydrin, epibromohydrin, β-
Methyl epichlorohydrin and the like are mentioned, and α-
Epihalogenohydrins can be used alone or as a mixture.

The tri (carboxyalkyl) isocyanurate represented by the general formula (2) is a polycarboxylic acid compound, and in the step a of the present invention, the compound represented by the general formula (2) is treated with α represented by the general formula (3). -A reaction in which epihalogenohydrin is added to obtain an ester. This reaction is carried out at room temperature using 3 to 30 mol, preferably 15 to 25 mol of α-epihalogenohydrin represented by general formula (3) per 1 mol of the compound of general formula (2). (About 20 ° C) ~
At 160 ° C., preferably at a temperature of 80-140 ° C.
It can react for 20 hours. As the catalyst, for example, tetramethylammonium chloride, tetraethylammonium bromide, quaternary onium salt such as n-butyltriphenylphosphonium bromide, or tertiary amine such as triethylamine, phosphine such as triphenylphosphine, sodium hydroxide, Potassium hydroxide,
Examples thereof include alkali metal hydroxides such as lithium hydroxide. These catalysts can be used alone or as a mixture, and the amount thereof is, relative to the compound of the general formula (2),
It can be used in a proportion of 0.001 to 10% by weight.

The step b of the present invention is a step of reacting the ester obtained in the step a with an alkaline substance. Examples of the alkaline substance include sodium hydroxide,
Examples thereof include alkali metal hydroxides of potassium hydroxide and lithium hydroxide, and these can be used alone or as a mixture. It is particularly preferable to use sodium hydroxide, and it can be used in the form of an aqueous solution. The amount of the alkaline substance to be used can be 3.0 to 6.0 mol per 1 mol of tri (carboxyalkyl) isocyanurate represented by the general formula (2). In this step b, it is preferable to react at a temperature of room temperature (about 20 ° C.) to 80 ° C. for 0.5 to 5 hours. At this time, the reaction can be carried out under atmospheric pressure, but water added by dropwise addition of an aqueous sodium hydroxide solution and water generated by the reaction are azeotroped with α-epihalogenohydrin which is present as an unreacted substance by excessive addition. 20 to 100 m inside the reaction vessel in order to remove it outside the reaction system.
It is preferable to maintain a reduced pressure of mHg. In step b, water and a salt are produced as by-products, but in order to suppress abnormal reaction and obtain an epoxy group in good yield, it is necessary to carry out the reaction while successively removing water from the reaction system. Thus, in step b, when the ester obtained in step a is reacted with the alkaline substance, dehydrohalogenation occurs from the ester obtained in step a, and the ester obtained in step a has 3 molecules in the molecule.
This produces an epoxy group to give the compound of the general formula (1) of the present invention.

General formula (1) of the present invention obtained in step b
The compound (2) coexists with a by-product salt and an alkali metal hydroxide when used in excess. To isolate the compound of the general formula (1) from these, sodium hydrogensulfate,
After the alkali metal hydroxide is made into a salt with a neutralizing agent such as sodium dihydrogen phosphate, the salt is removed by further washing with water, and then unreacted α-epihalogenohydrin due to excessive use is distilled off. Then impurities can be removed.

The epoxy compound represented by the general formula (1) of the present invention can be cured, that is, polymerized to obtain an epoxy resin cured product having excellent heat resistance and weather resistance. In the epoxy compound of the general formula (1), three Rs present in one molecule may be composed of only hydrogen atoms, may be composed of only methyl groups, or may be a combination of hydrogen atoms and methyl groups. The three n's present in one molecule may be composed of only an integer of 1 (methylene group), composed of only two integers (ethylene group), or may be a combination of integers of 1 and 2. These epoxy compounds of the general formula (1) can be used as the epoxy resin cured product of the present invention by curing alone or in combination of two or more. Further, in the present invention, the epoxy resin cured product of the present invention can be prepared by optionally using other epoxy resins such as bisphenol A diglycidyl ether type resin and phenol novolac epoxy resin in combination. Curing agent used at this time is an amine such as diaminodiphenylmethane, diaminodiphenylsulfone, methyl nadic acid anhydride, methyl hymic acid anhydride, hexahydrophthalic acid anhydride, tetrahydrophthalic acid anhydride, or the like, or Polyamide resin, polysulfide resin,
A complex of boron trifluoride and amine, dicyandiamide, may be mentioned. Further, the epoxy resin cured product includes fillers such as silica, alumina, talc and calcium carbonate, phosphorus-based flame retardants such as red phosphorus and phosphoric acid ester, halogen-based flame retardants such as chlorinated paraffin, and tertiary amines. A curing accelerator such as a quaternary ammonium salt, a tertiary phosphine or a quaternary phosphonium salt, or a toughness modifier such as rubber particles can be added.

[0026]

The epoxy compound represented by the general formula (1) of the present invention has three epoxy groups in one molecule and further has a rigid triazine skeleton in the molecule, so that the cured product has a glass transition temperature. The (Tg) is high, and therefore the temperature at which it is thermally deformed becomes high, and when it is an epoxy resin cured product, it has high heat resistance. The epoxy compound represented by the general formula (1) has a large binding energy because the main skeleton is a triazine ring, and has a lower ultraviolet absorption rate than the case where a benzene ring is used for the main skeleton, and the binding energy is Has good weather resistance. In particular, among the epoxy compounds represented by the general formula (1), the compound in which n is 1 has excellent heat resistance.

Among the epoxy compounds represented by the general formula (1) of the present invention, the compound in which n is 2 may cause a decomposition reaction depending on the standing condition. This is a slight amount of isocyanuric acid and the general formula (8) when the alkaline substance used in the step b in the production of the compound of the present invention remains.

[0028]

[Chemical 11]

(However, R ³ may represent a hydrogen atom or a methyl group.) May decompose into glycidyl acrylate. For example, after leaving the above-mentioned compound in which n is 2 for about 1 month in a state where the alkaline substance remains, ¹ H
-By measurement of NMR (proton nuclear magnetic resonance) spectrum, the characteristic spectrum derived from the vinyl group of glycidyl acrylate represented by the general formula (8) shows a proton integral around 6 ppm as a δ value from tetramethylsilane (internal standard). This can be confirmed by increasing the ratio. This n
In order to suppress the decomposition reaction of the compound of No. 2, it is necessary to sufficiently neutralize the epoxy compound of the general formula (1) obtained in step b with a neutralizing agent and then wash with water, and for a long period of time. It is desirable that the cured product of the epoxy resin be promptly prepared without storage.

The cured epoxy resin obtained by polymerizing the epoxy compound represented by the general formula (1) of the present invention is a bisphenol A diglycidyl ether type resin,
Compared with known resins such as phenol novolac epoxy resin and cresol novolac epoxy resin, it is more liquid at room temperature and has a smaller molecule aspect ratio, so that it has low viscosity during heating and excellent workability.

[0031]

【Example】

Example 1 Step a: 101 g of tri (carboxymethyl) isocyanurate, which is a compound of the general formula (2) and m is 1, is placed in a flask having an internal capacity of 1 liter equipped with a stirrer, a thermometer, a continuous dropping device and the like. [Corresponding to 0.33 mol], 625 g of α-epichlorohydrin [corresponding to 6.7 mol], and 3 g of tetramethylammonium chloride were added, and the mixture was stirred at 100 ° C. for 10 hours. During this period, the azeotropic vapor of α-epichlorohydrin and water was concentrated under reduced pressure so that only α-epichlorohydrin was returned to the reaction system.

Step b: The pressure inside the reaction system is reduced to 50 mmHg.
120 g of a 50% strength by weight caustic soda aqueous solution while maintaining the pressure in the reactor at 40 to 50 ° C.
[Equivalent to 1.5 mol] was added dropwise over 3 hours. During this period, the water in the aqueous caustic soda solution added dropwise and the water produced by the reaction were added in excess and existed as unreacted α
Removed out of the system by azeotroping with epichlorohydrin.

After the reaction is completed, the temperature in the reaction vessel is raised to room temperature.
Cool and add to 10 wt% sodium dihydrogen phosphate solution
Neutralize the caustic soda added in excess and then wash with water
To remove the by-product salts. And under reduced pressure (10m
mHg) Distilling off α-epichlorohydrin at 120 ° C
133 g of an epoxy compound was obtained. The yield is 84.9%
It was. This epoxy compound has an epoxy equivalent of 177 g.
/ Eq, a pale yellow viscous liquid. This epoxy
The compound has an IR (infrared absorption) spectrum measured by the KBr method.
As a result of setting, 910 cm^-1To the epoxy group
Income, 1690 cm ^-1Due to the carbonyl group of the triazine ring
Absorption coming, 1760 cm^-1To ester carbonyl group
The resulting absorption was observed. This IR spectrum is shown in FIG.
It was shown to. The epoxy compound obtained from this has the general formula
In the compound of (1), R is a hydrogen atom and n is 1.
Tri (carboxymethyl) isocyanurate, a compound
Triglycidyl ester [TCMICTG]
I confirmed the thing.

Example 2 Step a: In a flask having an internal volume of 1 liter equipped with a stirrer, a thermometer, a continuous dropping device, etc., tri (carboxymethyl) compound represented by the general formula (2) in which m is 1 101 g of isocyanurate [corresponding to 0.33 mol], 711 g of β-methylepichlorohydrin [corresponding to 6.7 mol],
Add 3 g of tetramethylammonium chloride and add 11
Stirred at 0 ° C. for 10 hours. During this period, the azeotropic vapor of β-methylepichlorohydrin and water was concentrated under reduced pressure, and only β-methylepichlorohydrin was returned to the reaction system.

Step b: Reduce the pressure in the reaction system to 50 mmHg
Of the caustic soda aqueous solution having a concentration of 50% by weight while maintaining the liquid temperature in the reaction vessel at 40 to 50 ° C.
[Equivalent to 1.3 mol] was added dropwise over 3 hours. During this period, the water in the aqueous caustic soda solution added dropwise and the water produced by the reaction were added in excess and existed as unreacted β
-Removed out of the system by azeotroping with methyl epichlorohydrin.

After completion of the reaction, the temperature in the reaction vessel was cooled to room temperature, the caustic soda added excessively was neutralized with an aqueous solution of 10% by weight sodium dihydrogen phosphate, and then washed with water to remove by-product salts. did. And under reduced pressure (10m
mHg) β-methylepichlorohydrin was distilled off at 120 ° C to obtain 157 g of an epoxy compound. Yield 92.0
%Met. This epoxy compound has an epoxy equivalent of 1
It was a pale yellow viscous liquid at 79 g / eq. This epoxy compound has an IR (infrared absorption) spectrum of KBr.
As a result of measurement by the method, absorption derived from an epoxy group was observed at 910 cm ⁻¹ , absorption derived from a carbonyl group of the triazine ring at 1690 cm ^−1, and absorption derived from an ester carbonyl group at 1760 cm ⁻¹ . This IR spectrum is shown in FIG. In addition, as a result of ¹ H-NMR (proton nuclear magnetic resonance) spectrum measurement in a magnetic field of 60 MHz using tetramethylsilane as an internal standard in a deuterated chloroform solvent, a δ value was 1.4 ppm and a β-methyl group was found. A peak derived from epoxymethylene group at 2.7 ppm, a peak derived from estermethylene group at 4.2 ppm, and a peak derived from carboxymethyl group at 4.7 ppm were observed. The NMR spectrum is shown in FIG. The epoxy compound thus obtained is a tri (carboxymethyl) isocyanurate triβ-methylglycidyl ester [TCMIC which is an epoxy compound in which R is a methyl group and n is 1 in the compound of the general formula (1).
β-MeTG] was confirmed.

Example 3 Step a: In a flask having an internal volume of 1 liter equipped with a stirrer, a thermometer, a continuous dropping device, etc., tri (carboxyethyl) compound of the general formula (2) in which m is 2 is shown. 115 g of isocyanurate [corresponding to 0.33 mol], 625 g of [alpha] -epichlorohydrin [corresponding to 6.7 mol] and 3 g of tetramethylammonium chloride were added and stirred at 100 [deg.] C. for 10 hours. During this period, the azeotropic vapor of α-epichlorohydrin and water was concentrated under reduced pressure so that only α-epichlorohydrin was returned to the reaction system.

Step b: The pressure inside the reaction system is reduced to 50 mmHg.
112 g of a 50% by weight aqueous solution of caustic soda while maintaining the liquid temperature in the reaction vessel at 40 to 50 ° C.
[Equivalent to 1.4 mol] was added dropwise over 3 hours. During this period, the water in the aqueous caustic soda solution added dropwise and the water produced by the reaction were added in excess and existed as unreacted α
Removed out of the system by azeotroping with epichlorohydrin.

After the completion of the reaction, the temperature in the reaction vessel was cooled to room temperature, the excessively added caustic soda was neutralized with a 10 wt% sodium dihydrogen phosphate aqueous solution, and then washed with water to remove salts of by-products. did. And under reduced pressure (10m
[alpha] -epichlorohydrin was distilled off at 120 [deg.] C. to obtain 147 g of an epoxy compound. The yield was 86.0%. This epoxy compound has an epoxy equivalent of 184 g.
/ Eq, a pale yellow viscous liquid. This epoxy compound was used in a deuterated chloroform solvent with tetramethylsilane as an internal standard in a magnetic field of 500 MHz for ¹ H.
As a result of measurement of -NMR (proton nuclear magnetic resonance) spectrum, peaks derived from epoxymethylene group at δ values of 2.6 ppm and 2.9 ppm, peaks derived from epoxymethine group at 3.2 ppm, 3.9 ppm and 4 .4p
Peak derived from ester methylene group at pm 2.7p
A peak derived from a carboxyethyl group was observed at pm and 4.2 ppm. The NMR spectrum is shown in FIG. It was confirmed that the epoxy compound thus obtained was tri (carboxyethyl) isocyanurate triglycidyl ester [TCEICTG], which is an epoxy compound in which R is a hydrogen atom and n is 2 in the compound of the general formula (1).

Example 4 Tri (carboxymethyl) isocyanurate triglycidyl ester, which is an epoxy compound of the general formula (1) obtained in Example 1 in which R is a hydrogen atom and n is 1, [abbreviated as T
CMICTG, the epoxy equivalent is 177 g / eq], and to one equivalent of the epoxy group, methylhymic acid anhydride [MHAC as abbreviation, molecular weight 178] is an acid anhydride.
Mixed at a ratio of 9 equivalents. This mixture at 80 ° C for 3
After mixing for 0 minutes with heating, tris (dimethylaminomethyl) phenol [trade name, D
MP-30] was mixed under deaeration under reduced pressure to obtain an epoxy resin composition. The mixing ratio of each component is shown in Table 1 in parts by weight.

This composition was heated in an oven at 100 ° C. for 2 hours and then at 180 ° C. for 3 hours to obtain an epoxy resin cured product. The heat resistance of this epoxy resin cured product was evaluated from the measured value of the glass transition temperature (Tg). The glass transition temperature (Tg) was measured from the change in thermal expansion of the cured product by thermomechanical analysis (TMA). The glass transition temperature (Tg) values are shown in Table 2.

Example 5 Instead of the epoxy compound obtained in Example 1, tri (carboxymethyl) which is an epoxy compound in which R in the general formula (1) obtained in Example 2 is a methyl group and n is 1 is obtained. Isocyanurate tri-β-methylglycidyl ester [TCMICβ-MeTG as abbreviation, epoxy equivalent is 179 g /
eq] was used, and the same procedure as in Example 4 was performed.

Example 6 Instead of the epoxy compound obtained in Example 1, tri (carboxyethyl) which is an epoxy compound of the general formula (1) obtained in Example 3 in which R is a hydrogen atom and n is 2. Isocyanurate triglycidyl ester [TCEI as abbreviation
The same procedure as in Example 4 was carried out except that CTG and epoxy equivalent were 184 g / eq.

Comparative Example 1 Commercially available bisphenol A diglycidyl ether type resin [BPAG as an abbreviation, epoxy equivalent 186 g / e
q, molecular weight 380] to 1 equivalent of an epoxy group, methylhymic acid anhydride which is an acid anhydride [abbreviated as MHA
C, molecular weight 178] were mixed in a ratio of 0.9 equivalent. This mixture was mixed with heating at 80 ° C. for 30 minutes, and then a curing accelerator tris (dimethylaminomethyl) phenol [trade name, DMP-30] was mixed under deaeration under reduced pressure to obtain an epoxy resin composition. I got a thing. The mixing ratio of each component is shown in Table 1 in parts by weight.

This composition was heated in an oven at 100 ° C. for 2 hours and then at 180 ° C. for 3 hours to obtain an epoxy resin cured product. The heat resistance of this epoxy resin cured product was evaluated from the measured value of the glass transition temperature (Tg). The glass transition temperature (Tg) was measured from the change in thermal expansion of the cured product by thermomechanical analysis (TMA). The glass transition temperature (Tg) values are shown in Table 2.

Table 1 Composition (parts by weight) Example 4 Example 5 Example 6 Comparative Example 1 TCMICTG 100 TCMIC β-MeTG 100 TCEICTG 100 BPAG 100 MHAC 90.5 89.5 87.1 84.3 DMP-30 3 3 3 3 Table 2 Example 4 Example Example 5 Comparative Example 1 Tg (° C.) 195 172 160 156 Example 7 Tri (carboxymethyl) which is an epoxy compound in which R in the general formula (1) obtained in Example 1 is a hydrogen atom and n is 1. Isocyanurate triglycidyl ester [abbreviated as T
CMICTG], tri (carboxymethyl) isocyanurate triβ-methylglycidyl ester [an abbreviation is TCMICβ-M, which is an epoxy compound in which R in the general formula (1) is a methyl group and n is 1 obtained in Example 2]
eTG] and the general formula (1) obtained in Example 3
The ultraviolet absorption (UV) spectrum of each epoxy compound of tri (carboxyethyl) isocyanurate triglycidyl ester [wherein R is a hydrogen atom and n is 2] [abbreviated as TCEICTG] was measured.
Each epoxy compound was measured at a concentration of 3 ppm. The measurement result is shown in FIG. In the spectrum in FIG. 5, TCEICTG and TCMITT are arranged in this order from the top on the left vertical axis.
G, TCMICβ-MeTG.

Comparative Example 2 Commercially available bisphenol A diglycidyl ether type resin [BPAG as abbreviation, epoxy equivalent 186 g / e
q, molecular weight 380] was measured for ultraviolet absorption (UV) spectrum. The measurement was performed in the same manner as in Example 7 at a concentration of 3 ppm. The measurement result is shown in FIG.

From Table 2, the epoxy resin cured product obtained by curing the epoxy compound represented by the general formula (1) of the present invention is obtained by curing a conventionally used bisphenol A diglycidyl ether type resin. Since it has a higher glass transition temperature than that of the cured epoxy resin, it has high heat resistance and is less prone to thermal deterioration. In particular, high heat resistance is obtained when using the epoxy compounds obtained in Examples 1 and 2.

Further, the epoxy compounds represented by the general formula (1) of the present invention obtained in Examples 1 to 3 from FIG. 5 have absorption of ultraviolet rays (wavelength near 300 nm) contained in sunlight. Since it is almost absent, it has good weather resistance when used as an epoxy resin cured product, and does not deteriorate even after long-term exposure. On the other hand, as shown in FIG. 6, the bisphenol A diglycidyl ether type resin has a slight absorption at a wavelength near 300 nm, so that photodegradation occurs due to long-term exposure. Further, in the ultraviolet region where the wavelength is shorter than 300 nm, the difference in absorption between the two becomes larger. The epoxy compound of the present invention can be preferably used in the electronic industry field utilizing the above-mentioned ultraviolet light, since it is less deteriorated by ultraviolet rays.

[0050]

The epoxy compound represented by the general formula (1) of the present invention has three epoxy groups in one molecule and further has a rigid triazine skeleton in the molecule, so that the glass transition temperature (Tg ) Is high, the temperature at which it thermally deforms is high, and it has high heat resistance when used as an epoxy resin cured product. Moreover, since the main skeleton is a triazine ring, the binding energy is large, and the ratio of ultraviolet absorption is low, so the weather resistance is good. In particular, the compound of the general formula (1) in which n is 1 is stable and exhibits extremely high heat resistance. In the present invention, the epoxy compound of the general formula (1) is an ester obtained by subjecting the tri (carboxyalkyl) isocyanurate of the general formula (2) to the α-epihalogenohydrin of the general formula (3). , Can be obtained in a high yield by a simple process by reacting with an alkaline substance. Since the epoxy resin cured product obtained by curing the epoxy compound of the general formula (1) has good heat resistance and weather resistance,
It can be used in the fields of paints, adhesives, various composite materials, and civil engineering and construction materials.

[Brief description of drawings]

1 shows an IR (infrared absorption) spectrum of the epoxy compound obtained in Example 1. FIG.

2 shows an IR (infrared absorption) spectrum of the epoxy compound obtained in Example 2. FIG.

FIG. 3 ¹ H—N of the epoxy compound obtained in Example 2
The MR (proton nuclear magnetic resonance) spectrum is shown.

FIG. 4 ¹ H—N of the epoxy compound obtained in Example 3
The MR (proton nuclear magnetic resonance) spectrum is shown.

FIG. 5 shows ultraviolet absorption (UV) spectra of the epoxy compounds obtained in Example 1, Example 2 and Example 3.

FIG. 6 shows an ultraviolet absorption (UV) spectrum of a bisphenol A diglycidyl ether type resin.

─────────────────────────────────────────────────── ─── Continuation of the front page (56) References Japanese Patent Publication No. 47-3533 (JP, B1) (58) Fields investigated (Int.Cl. ⁷ , DB name) C07D 405/14 REGISTRY (STN) CA (STN) )

Claims (4)

(57) [Claims] 1. The following general formula (1): (However, in the formula, R is a hydrogen atom or a methyl group, and n is 1
Or, an integer of 2 is shown. ) Epoxy compound represented by. 2. The epoxy compound according to claim 1, wherein n is an integer of 1 in the general formula (1). 3. The following a step and b step; a, the general formula (2); (However, in the formula, m represents an integer of 1 or 2.) In the tri (carboxyalkyl) isocyanurate,
General formula (3); (Provided that the R ¹ in the formula is a hydrogen atom or a methyl group, X ¹
Represents a halogen atom. The epoxy according to claim 1 or 2, further comprising a step of adding α-epihalogenohydrin represented by the formula (4) to obtain an ester, and a step of reacting the ester obtained in steps b and a with an alkaline substance. Method for producing compound. 4. An epoxy resin cured product obtained by curing the epoxy compound according to claim 1 or 2.