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Reaction of polyhalogenated unsaturated compounds with vanadium pentafluoride

Journal Article · · J. Org. Chem. USSR (Engl. Transl.); (United States)
OSTI ID:6250823
Terminal polyhalogenoalkenes are fluorinated by vanadium pentafluoride at -20 to -30/sup 0/C, whereas internal polyfluoroalkenes only react with vanadium pentafluoride when heated. 2-Chloropentafluoro-1,3-butadiene adds fluorine atoms predominantly at positions 1,4 under the influence of vanadium pentafluoride, but only the isomeric tetrafluorohexachlorobutanes are formed from perchloro-1,3-butadiene. Fluorination of perfluoroallylbenzene and perfluoro-..beta..-methylstyrene takes place more rapidly in the side chain than in the aromatic ring.
Research Organization:
Novosibirsk Institute of Organic Chemistry, USSR
OSTI ID:
6250823
Journal Information:
J. Org. Chem. USSR (Engl. Transl.); (United States), Journal Name: J. Org. Chem. USSR (Engl. Transl.); (United States) Vol. 23:1; ISSN JOCYA
Country of Publication:
United States
Language:
English

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