Synthesis 2004(14): 2277-2282  
DOI: 10.1055/s-2004-831177
PAPER
© Georg Thieme Verlag Stuttgart · New York

3-Acylindoles via a One-Pot, Regioselective Friedel-Crafts Reaction

James H. Wynnea,b, Christopher T. Lloyda, Samuel D. Jensena, Sean Bosonb, Wayne M. Stalick*b,c
a Chemistry Division, US Naval Research Laboratory, Washington, DC 20375, USA
b Department of Chemistry, George Mason University, Fairfax, VA 22030, USA
c Current address: Department of Chemistry, Central Missouri State University, Warrensburg, MO 64093, USA
Fax: +1(660)5434843; e-Mail: wstalick@gmu.edu;
Further Information

Publication History

Received 5 April 2004
Publication Date:
17 August 2004 (online)

Abstract

Within we report a general one-pot high-yielding Friedel-Crafts acylation of indole using acid chlorides and diethyl­aluminum chloride in gram scale quantities. This general synthesis affords products that are easily isolated and require no complex purification procedures.

1

Wynne, J. H.; Jones-Meehan, J. US Naval Research Laboratory, Washington, D. C., 2004, unpublished work.