Issue 41, 2010

Efficient and chemoselective alkylation of amines/amino acids using alcohols as alkylating reagents under mild conditions

Abstract

We report a mild and environmentally benign method for the synthesis of tertiary amines using alcohols as the alkylating reagents. Not only secondary amines such as piperazines but also amino acids and amino alcohols can be N-alkylated selectively. For N,O-benzyl protected amino alcohols, both N,O-de-benzylation and N-methylation were achieved in one-pot.

Graphical abstract: Efficient and chemoselective alkylation of amines/amino acids using alcohols as alkylating reagents under mild conditions

Supplementary files

Article information

Article type
Communication
Submitted
19 May 2010
Accepted
19 Jul 2010
First published
09 Sep 2010

Chem. Commun., 2010,46, 7834-7836

Efficient and chemoselective alkylation of amines/amino acids using alcohols as alkylating reagents under mild conditions

C. Xu, Z. Xiao, B. Zhuo, Y. Wang and P. Huang, Chem. Commun., 2010, 46, 7834 DOI: 10.1039/C0CC01487G

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