Synthesis 1988; 1988(11): 917-918
DOI: 10.1055/s-1988-27755
communication
© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved. This journal, including all individual contributions and illustrations published therein, is legally protected by copyright for the duration of the copyright period. Any use, exploitation or commercialization outside the narrow limits set by copyright legislation, without the publisher's consent, is illegal and liable to criminal prosecution. This applies in particular to photostat reproduction, copying, cyclostyling, mimeographing or duplication of any kind, translating, preparation of microfilms, and electronic data processing and storage.

A Simple and Economic Synthesis of Monoacylated Alkanediamines by Thermal Transamidation

Florencio Zaragoza-Dörwald* , Günter Von Kiedrowski
  • *Institut für Organische Chemie der Universität Göttingen, Tammannstraße 2, D-5300 Göttingen, Federal Republic of Germany
Further Information

Publication History

Publication Date:
20 August 2002 (online)

N-(ω-Aminoalkyl)amides 2 are easily synthesized by heating mixtures of excess α,ω-alkanediamines 1 and primary amides to temperatures between 150°C and 200°C, at which thermal transamidation occurs. Under the reaction conditions ammonia is released, and 2 is in equilibrium with the alkanediamine 1 and the α,ω-bis(acylamino)alkane 3. Thus, thermal transamidation is a practicable way to overcome the problem of diacylation which appears as an often recognized problem even in the latest literature.