Issue 0, 1972

Perfluoroalkyl derivatives of sulphur. Part XIV. The reactions of tetrafluoro-1,2-di-iodoethane and octafluoro-1,4-di-iodobutane with dimethyl sulphide and dimethyl disulphide

Abstract

The photochemical reaction of tetrafluoro-1,2-di-iodoethane with dimethyl sulphide gives a high yield of tetrafluoroethylene, whereas reaction with dimethyl disulphide affords 1,2-bis(methylthio)tetrafluoroethane and 1,4-bis-(methylthio)octafluorobutane as major products together with tetrafluoroethylene, methyl 1,1,2,2-tetrafluoroethyl sulphide, methyl tetrafluoro-2-iodoethyl sulphide, perfluorocyclopropane, and difluoromethane. Octafluoro-1,4-di-iodobutane and dimethyl sulphide give 1H-octafluoro-4-iodobutane, methyl octafluoro-4-iodobutyl sulphide, and trimethylsulphonium iodide as the major products with smaller amounts of 1H,4H-octafluoro-butane, 1,4-bis(methylthio)octafluorobutane, and methyl 4H-octafluorobutyl sulphide.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1972, 2438-2441

Perfluoroalkyl derivatives of sulphur. Part XIV. The reactions of tetrafluoro-1,2-di-iodoethane and octafluoro-1,4-di-iodobutane with dimethyl sulphide and dimethyl disulphide

R. N. Haszeldine, R. B. Rigby and A. E. Tipping, J. Chem. Soc., Perkin Trans. 1, 1972, 2438 DOI: 10.1039/P19720002438

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