Synlett 2002(3): 0528-0530
DOI: 10.1055/s-2002-20487
LETTER
© Georg Thieme Verlag Stuttgart · New York

A Conceptually New and Straightforward Method for the One-pot Transformation of Alcohols into Amines

V. Gasparik, V. Dalla*, B. Decroix
Unité de Recherche en Chimie Organique et Macromoléculaire, Faculté des Sciences et Techniques de l’Université du Havre, 25 rue Philippe Lebon, BP 540, 76058 Le Havre cedex, France
Fax: +33(2)32744391; e-Mail: vincent.dalla@univ-lehavre.fr;
Further Information

Publication History

Received 18 December 2001
Publication Date:
05 February 2007 (online)

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Abstract

A conceptually new amination method of alcohols has been developed using α-hydroxy esters as substrates and N-phenyl bis-trifluoromethanesulfonimide (PhNTf2) as a test reagent. Playing two roles at once, PhNTf2 activates the hydroxyl group as a highly reactive triflate intermediate and introduces the amino functionality through an in situ nucleophilic substitution by the anionic residue PhTfN-. Two complementary procedures (methods A and B herein) have been developed, the latter permitting reaction of substrates with unstable alcoxides.