Synlett 2006(18): 3176-3178  
DOI: 10.1055/s-2006-948192
LETTER
© Georg Thieme Verlag Stuttgart · New York

One-Pot Halogenation-Heck Coupling Reactions in Ionic Liquids

Scott T. Handy*
Department of Chemistry, Middle Tennessee State University, Murfreesboro, TN 37132, USA
Fax: +1(615)8985182; e-Mail: shandy@mtsu.edu;
Further Information

Publication History

Received 27 March 2006
Publication Date:
04 August 2006 (online)

Abstract

Traditional cross-coupling approaches rely upon two steps - halogenation and coupling - each of which is viewed and conducted independently. In an effort to develop a one-pot ­approach, we have noted that the halogenation and Heck coupling reactions can both be conducted in a room-temperature ionic liquid without the need to isolate the halogenated intermediate. Application to several systems shows that this approach works well for moderately to highly electron-rich aromatics.

7

It is worth noting that the regioselectivity reported for these halogenations in RTILs is also quite high. In the halogenation-couplings reported in this work, no trace of any regioisomeric products could be detected by 1H NMR.

9

All of the products reported exhibit spectral properties consistent with those reported in the literature.