Home
About
Editorial Board
Instructions to Authors
Subscription
Archive
Proceeding
Submission
Citation Data
Advertising
Feedback


J. Iran. Chem. Soc., Vol. 2, No. 4 December 2005, pp.315~318.

Current location: JICS Archive > Vol. 2 > No. 4 > Articles : 6

Synthesis of Triphenylmethylphosphonium Chlorochoromate as A Mild and Selective Reagent for Oxidation of Alcohols


A.R. Hajipoura,b,*, L. Khazdooza and A.E. Ruohob


aPharmaceutical Research Laboratory, College of Chemistry, Isfahan University of Technology, Isfahan 84156, Iran
bDepartment of Pharmacology, University of Wisconsin Med. Sch. 1300 University Avenue, Madison, 53706-1532, WI, USA


Triphenylmethylphosphonium chlorochoromate was synthesized from triphenylmethyl bromide and chromium(VI) oxide in HCl 6 N and used as an efficient and selective reagent for oxidation of alcohols to their corresponding aldehydes or ketones derivatives in refluxing acetonitrile in good to excellent yields.


Keywords: Alcohols, Aldehydes, Ketones, Oxidation, Triphenylmethylphosphonium chlorochoromate

Download full-text PDF