JPS6490180A - Epoxy compound and production thereof - Google Patents

Epoxy compound and production thereof

Info

Publication number
JPS6490180A
JPS6490180A JP24868187A JP24868187A JPS6490180A JP S6490180 A JPS6490180 A JP S6490180A JP 24868187 A JP24868187 A JP 24868187A JP 24868187 A JP24868187 A JP 24868187A JP S6490180 A JPS6490180 A JP S6490180A
Authority
JP
Japan
Prior art keywords
formula
compound expressed
expressed
reacted
production
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP24868187A
Other languages
Japanese (ja)
Inventor
Noriyuki Ogami
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Idemitsu Petrochemical Co Ltd
Original Assignee
Idemitsu Petrochemical Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Idemitsu Petrochemical Co Ltd filed Critical Idemitsu Petrochemical Co Ltd
Priority to JP24868187A priority Critical patent/JPS6490180A/en
Publication of JPS6490180A publication Critical patent/JPS6490180A/en
Pending legal-status Critical Current

Links

Abstract

NEW MATERIAL:A compound expressed by formula I (R<1> is 6-20C alkyl; R<2> is hexamethylene or tolylene). EXAMPLE:A compound expressed by formula IV. USE:A raw material and flexibilizer for epoxy resins, stabilizer for vinyl chloride resin, etc., having alkyl groups of a relatively long chain and excellent reactivity. PREPARATION:A diisocyanate compound expressed by formula II is reacted with alcohols expressed by the formula R<1>OH at 0-100 deg.C for 30min-5hr to provide a dicarbamate compound expressed by formula III, which is then reacted in the presence of an epihalohydrin and an alkali, such as NaOH, as necessary, coexisting with a catalyst, such as tetra-n-butylammonium hydrosulfate, and an azeotropic solvent, such as benzene, under reduced pressure, preferably at 40-60 deg.C while being heated and refluxed to readily afford the aimed compound expressed by formula I in high yield.
JP24868187A 1987-09-30 1987-09-30 Epoxy compound and production thereof Pending JPS6490180A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP24868187A JPS6490180A (en) 1987-09-30 1987-09-30 Epoxy compound and production thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP24868187A JPS6490180A (en) 1987-09-30 1987-09-30 Epoxy compound and production thereof

Publications (1)

Publication Number Publication Date
JPS6490180A true JPS6490180A (en) 1989-04-06

Family

ID=17181746

Family Applications (1)

Application Number Title Priority Date Filing Date
JP24868187A Pending JPS6490180A (en) 1987-09-30 1987-09-30 Epoxy compound and production thereof

Country Status (1)

Country Link
JP (1) JPS6490180A (en)

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