An alternative route to syntheses of aryl keto acids in a chloroaluminate ionic liquid

8Citations
Citations of this article
6Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

The Lewis acidic 1-butyl-3-methylimidazolium chloroaluminate ionic liquid [bmim]Cl.AlCl3, N=0.67, is employed as a catalyst as well as the solvent for the quick and efficient syntheses of aryl keto acids by Friedel-Crafts acylation and aroylation of aromatic hydrocarbons using cyclic acid anhydrides.

Cite

CITATION STYLE

APA

Mohile, S. S., Potdar, M. K., & Salunkhe, M. M. (2003). An alternative route to syntheses of aryl keto acids in a chloroaluminate ionic liquid. Journal of Chemical Research - Part S, (10), 650–651. https://doi.org/10.3184/030823403322655969

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free