JPS6456655A - Production of 3,3-dimethyl-2-bromobutylonitrile - Google Patents

Production of 3,3-dimethyl-2-bromobutylonitrile

Info

Publication number
JPS6456655A
JPS6456655A JP21368487A JP21368487A JPS6456655A JP S6456655 A JPS6456655 A JP S6456655A JP 21368487 A JP21368487 A JP 21368487A JP 21368487 A JP21368487 A JP 21368487A JP S6456655 A JPS6456655 A JP S6456655A
Authority
JP
Japan
Prior art keywords
dimethylbutylonitrile
reaction
bromine
times mol
pressure system
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
JP21368487A
Other languages
Japanese (ja)
Inventor
Kazuo Tashiro
Keiko Adachi
Michio Yamato
Shinzaburo Masaki
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.)
Sumitomo Chemical Co Ltd
Original Assignee
Sumitomo Chemical 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 Sumitomo Chemical Co Ltd filed Critical Sumitomo Chemical Co Ltd
Priority to JP21368487A priority Critical patent/JPS6456655A/en
Publication of JPS6456655A publication Critical patent/JPS6456655A/en
Pending legal-status Critical Current

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  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

PURPOSE:To obtain a compound useful as a synthetic intermediate for agricultural chemical, etc., without requiring troublesome process in high selectivity and yield. CONSTITUTION:3,3-Dimethylbutylonitrile is reacted with bromine, preferably without solvent at 80-200 deg.C to provide the aimed product. The bromine is used at an amount of 0.1-2 times mol., especially preferably 0.1-1.1 times mol. based on 3,3-dimethylbutylonitrile. Bromination reaction may be carried out also using an organic solvent such as chloroform and as pressure in reaction, ordinary pressure system or pressure system can be applied. 3,3- Dimethylbutylonitrile raw material is readily obtainable by reaction of tert.- butylbromide with acetonitrile.
JP21368487A 1987-08-26 1987-08-26 Production of 3,3-dimethyl-2-bromobutylonitrile Pending JPS6456655A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP21368487A JPS6456655A (en) 1987-08-26 1987-08-26 Production of 3,3-dimethyl-2-bromobutylonitrile

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP21368487A JPS6456655A (en) 1987-08-26 1987-08-26 Production of 3,3-dimethyl-2-bromobutylonitrile

Publications (1)

Publication Number Publication Date
JPS6456655A true JPS6456655A (en) 1989-03-03

Family

ID=16643269

Family Applications (1)

Application Number Title Priority Date Filing Date
JP21368487A Pending JPS6456655A (en) 1987-08-26 1987-08-26 Production of 3,3-dimethyl-2-bromobutylonitrile

Country Status (1)

Country Link
JP (1) JPS6456655A (en)

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