A Triple Newman-Kwart Rearrangement at a Fully Substituted Benzene Ring

Author:

Theil Hubert1,Fröhlich Roland2,Glaser Thorsten1

Affiliation:

1. Fakultät für Chemie, Universität Bielefeld, Universitätsstr. 25, D-33615 Bielefeld, Germany

2. Organisch-Chemisches Institut, Westfälische Wilhelms-Universität D-Münster, Corrensstr. 40, 48149 Münster, Germany

Abstract

The Newman-Kwart rearrangement of O-thiocarbamates to S-thiocarbamates is a versatile method for the conversion of phenols into thiophenols. The triple rearrangement of the O-trithiocarbamate 2,4,6-triacetyl-1,3,5-tri-(dimethylthiocarbamoyloxy)benzene (2) to the S-trithiocarbamate 2,4,6- triacetyl-1,3,5-tri-(dimethylthiocarbamoylthio)benzene (3) is performed, which is unprecendented for fully substituted benzene rings. The synthesis and characterization of the O-trithiocarbamate 2 and the S-trithiocarbamate 3 including the single-crystal X-ray structure analysis of compound 3 are presented

Publisher

Walter de Gruyter GmbH

Subject

General Chemistry

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