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Synthesis 2010(17): 2990-2996
DOI: 10.1055/s-0030-1258158
DOI: 10.1055/s-0030-1258158
PAPER
© Georg Thieme Verlag
Stuttgart ˙ New York1-Propanephosphonic Acid Cyclic Anhydride (T3P) as an Efficient Promoter for the Lossen Rearrangement: Application to the Synthesis of Urea and Carbamate Derivatives
Further Information
Received
30 March 2010
Publication Date:
07 July 2010 (online)
Publication History
Publication Date:
07 July 2010 (online)

Abstract
The synthesis of hydroxamic acids starting from carboxylic acids employing 1-propanephosphonic acid cyclic anhydride (T3P) activation is described. Application of ultrasonication accelerates this conversion. Further, the T3P has also been employed to activate the hydroxamates, leading to isocyanates via the Lossen rearrangement. The isocyanates were trapped with suitable nucleophiles to afford the corresponding ureas and carbamates.
Key words
T3P - hydroxamic acids - Lossen rearrangement - isocyanates
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