Synthesis 1988; 1988(12): 1007-1009
DOI: 10.1055/s-1988-27789
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.

A Simple and Efficient Synthesis of Alkyl (2-Nitroaryl)acetates and Alkyl 2-(2-Nitroaryl)propanoates via Vicarious Nucleophilic Substitution of Hydrogen in Nitroarenes by Carbanions or Alkyl Chloroacetates of Alkyl 2-Chloropropanoates

B. Mudryk* , M. Mąkosza
  • *Institute of Organic Chemistry, Polish Academy of Science, ul. Kasprzaka 44/52, PL 01-224 Warsaw, Poland
Further Information

Publication History

Publication Date:
20 August 2002 (online)

Alkyl chloroacetates react with nitroarenes and potassium tert-butoxide in dimethylformamide according to the Vicarious Nucleophilic Substitution pattern, preferentially in the position ortho to the nitro group, giving alkyl (2-nitroaryl)acetates in usually good yields. Alkyl 2-(2-nitroaryl) propanoates are obtained in an analogous manner.

    >