Synthesis 2013; 45(8): 1069-1075
DOI: 10.1055/s-0032-1318477
paper
© Georg Thieme Verlag Stuttgart · New York

Facile Synthesis of N-Substituted Amides from Alcohols and Amides

Iku Okada
Laboratory of Bio-organic Chemistry, Tokyo University of Agriculture and Technology, 3-5-8 Saiwai-cho, Fuchu-shi, Tokyo 183-8509, Japan   Fax: +81(42)3675700   Email: kitayo@cc.tuat.ac.jp
,
Kazuhiro Chiba
Laboratory of Bio-organic Chemistry, Tokyo University of Agriculture and Technology, 3-5-8 Saiwai-cho, Fuchu-shi, Tokyo 183-8509, Japan   Fax: +81(42)3675700   Email: kitayo@cc.tuat.ac.jp
,
Yoshikazu Kitano*
Laboratory of Bio-organic Chemistry, Tokyo University of Agriculture and Technology, 3-5-8 Saiwai-cho, Fuchu-shi, Tokyo 183-8509, Japan   Fax: +81(42)3675700   Email: kitayo@cc.tuat.ac.jp
› Author Affiliations
Further Information

Publication History

Received: 18 January 2013

Accepted after revision: 25 February 2013

Publication Date:
18 March 2013 (online)


Abstract

A facile and versatile method for preparing N-substituted amides from alcohols and amides using a Brønsted acid and an alkali metal halide has been developed. Treatment of tertiary alcohols and amides in the presence of an alkali metal halide or methanesulfonic acid in trifluoroacetic acid at elevated temperature afforded the corresponding N-substituted amides in moderate to high yields. Tertiary alcohols with various functional groups such as ether, ester, imide, carbamate, and halogen groups were tolerated under these conditions. This method can be used for the efficient and practical synthesis of various N-substituted formamides without the use of unmanageable cyano compounds.

Supporting Information

 
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