Abstract

The reaction of perfluoro(4-ethyl-3,4-dimethylhex-2-ene) (TFE pentamer) with sodium azide in acetonitrile afforded perfluoro[2,3-dimethyl-2-(3-methylpentan-3-yl)]-2H-azirine as a stable distillable liquid. The azirine reacted slowly with nucleophiles to give a series of substituted 2,3-bis-(trifluoromethyl)aziridines. A rationale of this somewhat unexpected reaction is suggested.

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