Synlett 2005(2): 322-324  
DOI: 10.1055/s-2004-836062
LETTER
© Georg Thieme Verlag Stuttgart · New York

HCl-Catalyzed Stereoselective Mannich Reaction in H2O-SDS System

Takahiko Akiyama*, Keiichiro Matsuda, Kohei Fuchibe
Department of Chemistry, Faculty of Science, Gakushuin University, 1-5-1 Mejiro, Toshima-ku, Tokyo 171-8588, Japan
Fax: +81(3)59921029; e-Mail: takahiko.akiyama@gakushuin.ac.jp;
Further Information

Publication History

Received 19 October 2004
Publication Date:
10 December 2004 (online)

Abstract

HCl-catalyzed Mannich reaction of cyclic ketone, aromatic aldehyde, and aromatic amine proceeded smoothly in water in the presence of SDS to afford the corresponding β-amino ketone with high anti selectivity.

11

Although Brønsted acid-catalyzed Mannich reactions have been reported, [9] [10] high stereoselectivity has not been observed.

12

We have not observed the diaminoalkylation product.

13

Other acyclic ketones such as 2-butanone and propiophenone did not give the Mannich adduct.