Synthesis 1986; 1986(10): 868-870
DOI: 10.1055/s-1986-31813
communication
© 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.

Synthetic Methods and Reactions; 1271. Regioselective para Halogenation of Phenols, Phenol Ethers and Anilines with Halodimethylsulfonium Halides

George A. Olah* , Lena Ohannesian, Massoud Arvanaghi
  • *Donald P. and Katherine B. Loker Hydrocarbon Research Institute and Department of Chemistry, University of Southern California, Los Angeles, CA 90089-1661, U. S. A.
Further Information

Publication History

Publication Date:
20 August 2002 (online)

Halodimethylsulfonium halides [bromodimethylsulfonium bromide and chlorodimethylsulfonium chloride] are efficient regioselective para halogenating agent for activated aromatics, such as phenol, anisole, diphenyl ether and N-alkylanilines. Dihalo and monohalo derivatives of diphenyl ethers were obtained depending upon the reaction conditions. Aniline itself is not suitable in the reaction due to the strong complexation of the lone electron pair of nitrogen with the sulfonium reagent.

    >