Synthesis 2003(4): 0565-0569
DOI: 10.1055/s-2003-37651
PAPER
© Georg Thieme Verlag Stuttgart · New York

The Preparation of Aliphatic Fluorinated Sulfoximines

Emmanuel Magnier, Claude Wakselman*
SIRCOB-CNRS, Bâtiment Lavoisier, Université de Versailles-Saint-Quentin, 45 avenue des Etats-Unis, 78035 Versailles, France
Fax: +33(1)39254452; e-Mail: wakselma@chimie.uvsq.fr;
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Publikationsverlauf

Received 22 October 2002
Publikationsdatum:
07. März 2003 (online)

Abstract

This work describes the preparation of an aliphatic series of the N-trifluoromethanesulfonyl-S-trifluoromethyl-S-sulfoximine group. The key step of the synthesis is the imination of fluorinated sulfoxides under experimental conditions, which avoid cleavage of the alkyl group. The formation of sulfoximines 6 and 15 allows the preparation of various fluorinated sulfoximines having strong electron withdrawing properties.

10

We assume that the lack of reactivity is due to the poor nucleophilicity of the sulfur because of the presence of the trifluoromethyl group.

12

Attempts at imination of sulfoxide 5 under Yagupol’skii’s conditions gave rise to a complex mixture of products in a low yield. In Bentley and Whitehead’s conditions no transformation of the fluorinated sulfoxide 5 was observed.