Synlett 2013; 24(17): 2249-2254
DOI: 10.1055/s-0033-1339667
letter
© Georg Thieme Verlag Stuttgart · New York

Use of Primary Amines for the Selective N-Alkylation of Anilines by a Reusable Heterogeneous Catalyst

Pasquale Linciano
a   Dipartimento di Biotecnologie, Chimica e Farmacia, Università degli Studi di Siena, Via A. Moro 2, 53100 Siena, Italy   Fax: +39(057)7234333   Email: taddei.m@unisi.it
,
Marianna Pizzetti
a   Dipartimento di Biotecnologie, Chimica e Farmacia, Università degli Studi di Siena, Via A. Moro 2, 53100 Siena, Italy   Fax: +39(057)7234333   Email: taddei.m@unisi.it
,
Andrea Porcheddu
b   Dipartimento di Chimica e Farmacia, Via Vienna 2, 07100 Sassari, Italy
,
Maurizio Taddei*
a   Dipartimento di Biotecnologie, Chimica e Farmacia, Università degli Studi di Siena, Via A. Moro 2, 53100 Siena, Italy   Fax: +39(057)7234333   Email: taddei.m@unisi.it
› Author Affiliations
Further Information

Publication History

Received: 26 June 2013

Accepted after revision: 02 August 2013

Publication Date:
13 September 2013 (online)


Preview

Abstract

Traditionally, anilines can be alkylated with reactive alkyl halides but now more safe reagents such as alcohols or even amines can be used. To overcome the limits of homogeneous catalysis for aniline N-alkylation, we have developed a protocol that employs simple Pd/C as a heterogeneous catalyst under microwave dielectric heating. The process, based on the easy Pd-mediated oxidation of primary amines to imines followed by aniline addition, is characterized by a high atom economy as ammonia is the only other product of the reaction. This kind of aniline alkylation with amines has been carried out both in ionic liquid medium using [bmim]PF6 or in a more traditional solvent such as THF where the catalyst could be successfully recycled more times. The reusability of the catalyst was further confirmed by using material recycled from the amination in a standard alkene hydrogenation without loss of efficiency.

Supporting Information