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Synthesis 2013; 45(2): 231-236
DOI: 10.1055/s-0032-1317927
DOI: 10.1055/s-0032-1317927
paper
A User-Friendly Procedure for the Preparation of Secondary Alkyl Chlorides
Weitere Informationen
Publikationsverlauf
Received: 19. November 2012
Accepted: 26. November 2012
Publikationsdatum:
19. Dezember 2012 (online)
Abstract
Secondary alkyl chlorides have been efficiently prepared from secondary alkyl sulfonates under mild and user-friendly conditions. The exchange reaction was generally performed by using benzyltributylammonium chloride in acetone (reflux, 30 min). Yields are excellent from functionalized, base-sensitive and hindered secondary alkyl sulfonates.
Key words
nucleophilic substitution - sulfonates - secondary alkyl chlorides - quaternary ammonium halides - sulfonate–halogen exchangeSupporting Information
- for this article is available online at http://www.thieme-connect.com/ejournals/toc/synthesis.
- Supporting Information
-
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For general reviews on cross-coupling reactions with alkyl halides, see:
For some immobilized tertiary ammonium derivatives, see:
For metal salt catalyzed procedures, see: