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Synthesis 2008(11): 1679-1681
DOI: 10.1055/s-2008-1067040
DOI: 10.1055/s-2008-1067040
SHORTPAPER
© Georg Thieme Verlag Stuttgart · New York
Rapid and Convenient Microwave-Assisted Synthesis of Primary Amines via Reductive N-Alkylation of Methyl Carbamate with Aldehydes
Weitere Informationen
Received
20 February 2008
Publikationsdatum:
29. April 2008 (online)
Publikationsverlauf
Publikationsdatum:
29. April 2008 (online)

Abstract
Microwave-assisted reductive alkylation of methyl carbamate with a range of aldehydes provides, after basic work-up, an experimentally simple, one-pot method for rapid functional group interconversion of structurally diverse aldehydes into primary amines. The method has several advantages over more traditional methods of carrying out this transformation and is particularly amenable to high-throughput synthesis.
Key words
aminations - aldehydes - reductive alkylation - carbamates - amines - microwave synthesis
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