JPS6440443A - Fluoroether compound and production thereof - Google Patents

Fluoroether compound and production thereof

Info

Publication number
JPS6440443A
JPS6440443A JP19637987A JP19637987A JPS6440443A JP S6440443 A JPS6440443 A JP S6440443A JP 19637987 A JP19637987 A JP 19637987A JP 19637987 A JP19637987 A JP 19637987A JP S6440443 A JPS6440443 A JP S6440443A
Authority
JP
Japan
Prior art keywords
formula
perfluoroalkyl
compound shown
aryl
halogen
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.)
Granted
Application number
JP19637987A
Other languages
Japanese (ja)
Other versions
JPH0788331B2 (en
Inventor
Yuji Izeki
Masahiro Takesue
Kuniaki Takada
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.)
Tokuyama Corp
Original Assignee
Tokuyama Corp
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 Tokuyama Corp filed Critical Tokuyama Corp
Priority to JP19637987A priority Critical patent/JPH0788331B2/en
Publication of JPS6440443A publication Critical patent/JPS6440443A/en
Publication of JPH0788331B2 publication Critical patent/JPH0788331B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

Abstract

NEW MATERIAL:A fluoroether compound shown by formula I [Y is halogen, perfluoroalkyl or OR1 (R1 is alkyl, aryl or perfluoroalkyl); R is alkyl, aryl or perfluoroalkyl; X is acid group, group readily replaceable with acid group, halogen or group shown by formula II (Y' is halogen, perfluoroalkyl or OR1; R' is alkyl, aryl or perfluoroalkyl; l is >=0 integer); m is >=1 integer; n is >=0 integer]. EXAMPLE:A compound shown by formula III. USE:A raw material for fluorodivinyl etherified substances and a fluoropolyvinyl ether compound which can substantially improve crosslinking density. PREPARATION:A fluorocarboxylic acid fluoride shown by formula IV is reacted with an epoxy compound shown by formula V in the presence of a fluorine ion forming catalyst to give a fluoroether compound shown by formula I.
JP19637987A 1987-08-07 1987-08-07 Fluoroether compound and method for producing the same Expired - Lifetime JPH0788331B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP19637987A JPH0788331B2 (en) 1987-08-07 1987-08-07 Fluoroether compound and method for producing the same

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP19637987A JPH0788331B2 (en) 1987-08-07 1987-08-07 Fluoroether compound and method for producing the same

Publications (2)

Publication Number Publication Date
JPS6440443A true JPS6440443A (en) 1989-02-10
JPH0788331B2 JPH0788331B2 (en) 1995-09-27

Family

ID=16356891

Family Applications (1)

Application Number Title Priority Date Filing Date
JP19637987A Expired - Lifetime JPH0788331B2 (en) 1987-08-07 1987-08-07 Fluoroether compound and method for producing the same

Country Status (1)

Country Link
JP (1) JPH0788331B2 (en)

Also Published As

Publication number Publication date
JPH0788331B2 (en) 1995-09-27

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