JPS5444624A - Di-2,4-dinitrophenyl 3,4-epoxyadipate - Google Patents

Di-2,4-dinitrophenyl 3,4-epoxyadipate

Info

Publication number
JPS5444624A
JPS5444624A JP10926177A JP10926177A JPS5444624A JP S5444624 A JPS5444624 A JP S5444624A JP 10926177 A JP10926177 A JP 10926177A JP 10926177 A JP10926177 A JP 10926177A JP S5444624 A JPS5444624 A JP S5444624A
Authority
JP
Japan
Prior art keywords
dinitrophenyl
formula
room temperature
epoxyadipate
hexenedioic
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
JP10926177A
Other languages
Japanese (ja)
Inventor
Yasuyuki Shimozato
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.)
JSR Corp
Original Assignee
Japan Synthetic Rubber 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 Japan Synthetic Rubber Co Ltd filed Critical Japan Synthetic Rubber Co Ltd
Priority to JP10926177A priority Critical patent/JPS5444624A/en
Publication of JPS5444624A publication Critical patent/JPS5444624A/en
Pending legal-status Critical Current

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  • Epoxy Compounds (AREA)

Abstract

NEW MATERIAL:Di-2,4-dinitrophenyl 3,4-epoxyadipate of formula IV.
EXAMPLE: Di-2,4-dinitrophenyl trans-3,4-epoxyadipate.
USE: Synthesis of polyamides bearing epoxy groups. As the compound is highly reactive the reaction can be effected near room temperature.
PREPARATION: For example, 3-hexenedioic acid of formulaIis reacted with phosphorus pentachloride at room temperature to form 3-hexenedioic dichloride of formula II, which is converted to di-2,4-dinitrophenyl 3-hexenedioate of formula III by reacting with 2,4-dinitrophenol in acetone in the presence of triethylamine at room temperature for 24hr. The resulting product is heated togther with m-chloroperbenzioc acid in benzene under refluxing to prepare the objective compound of formula IV.
COPYRIGHT: (C)1979,JPO&Japio
JP10926177A 1977-09-09 1977-09-09 Di-2,4-dinitrophenyl 3,4-epoxyadipate Pending JPS5444624A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP10926177A JPS5444624A (en) 1977-09-09 1977-09-09 Di-2,4-dinitrophenyl 3,4-epoxyadipate

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP10926177A JPS5444624A (en) 1977-09-09 1977-09-09 Di-2,4-dinitrophenyl 3,4-epoxyadipate

Publications (1)

Publication Number Publication Date
JPS5444624A true JPS5444624A (en) 1979-04-09

Family

ID=14505682

Family Applications (1)

Application Number Title Priority Date Filing Date
JP10926177A Pending JPS5444624A (en) 1977-09-09 1977-09-09 Di-2,4-dinitrophenyl 3,4-epoxyadipate

Country Status (1)

Country Link
JP (1) JPS5444624A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6146624A (en) * 1984-08-10 1986-03-06 Sony Corp Error correcting device
US5319113A (en) * 1992-08-28 1994-06-07 The Aerospace Corporation Preparation of liquid crystalline di(alkoxyglycidyl) compounds, and their use in curable epoxide mixtures

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6146624A (en) * 1984-08-10 1986-03-06 Sony Corp Error correcting device
US5319113A (en) * 1992-08-28 1994-06-07 The Aerospace Corporation Preparation of liquid crystalline di(alkoxyglycidyl) compounds, and their use in curable epoxide mixtures

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