Synthesis 1993; 1993(6): 573-574
DOI: 10.1055/s-1993-25907
short paper
© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved. This journal, including all individual contributions and illustrations published therein, is legally protected by copyright for the duration of the copyright period. Any use, exploitation or commercialization outside the narrow limits set by copyright legislation, without the publisher's consent, is illegal and liable to criminal prosecution. This applies in particular to photostat reproduction, copying, cyclostyling, mimeographing or duplication of any kind, translating, preparation of microfilms, and electronic data processing and storage.

Oxidative Cleavage of Aryl or Alkyl tert-Butyl Sulfides with Dimethyl Sulfoxide/Hydrobromic Acid to Form Symmetrical Aryl or Alkyl Disulfides

Daniel A. Dickman* , Sanjay Chemburkar, Donald B. Konopacki, E. Michael Elisseou
  • *Process Research, Pharmaceutical Products Division, Abbott Laboratories, One Abbott Park Road, Abbott Park, Illinois 60064, USA
Further Information

Publication History

Publication Date:
17 September 2002 (online)

The use of dimethyl sulfoxide and hydrobromic acid as a reagent to oxidatively cleave (tert-butylthio)benzaldehydes, aryl or alkyl tert-butyl sulfides to their corresponding symmetrical disulfides is discussed. A brief mechanistic rationale is given based upon several control experiments.

    >