Abstract

Preparation of the First Thione S‐Imides with Perfluoromethyl Groups by the Use of Sodium Hexamethyldisilazanide as a Mild Dehydrohalogenation ReagentFrom the reaction of the sulfenyl chloride 1 with the monosilylated amines 2a, b the sulfenamides 3a, b are obtained in good yields. 1,3‐Dehydrohalogenation of 3a, b with sodium hexamethyldisilazanide yields the thione S‐imides 5a, b. Imide 5a reacts with norbornene (6) to produce the isothiazolidine derivative 7. The structures of 5b and 7 are confirmed by X‐ray analyses.

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