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Article
Access to Aryl Mellitic Acid Esters through a Surprising Oxidative Esterification Reaction
The Journal of Organic Chemistry
  • Margarita R. Geraskina, Iowa State University
  • Mark James Juetten, Iowa State University
  • Arthur Winter, Iowa State University
Document Type
Article
Publication Version
Published Version
Publication Date
1-1-2014
DOI
10.1021/jo5005185
Abstract

A serendipitously discovered oxidative esterification reaction of cyclohexane hexacarboxylic acid with phosphorus pentachloride and phenols provides one-pot access to previously unknown aryl mellitic acid esters. The reaction features a solvent-free digestion and chromatography-free purifications and demonstrates the possibility of cyclohexane-to-benzene conversions under relatively mild, metal-free conditions.

Comments

Reprinted (adapted) with permission from J. Org. Chem., 2014, 79 (11), pp 5334–5337. Copyright 2014 American Chemical Society.

Copyright Owner
American Chemical Society
Language
en
File Format
application/pdf
Citation Information
Margarita R. Geraskina, Mark James Juetten and Arthur Winter. "Access to Aryl Mellitic Acid Esters through a Surprising Oxidative Esterification Reaction" The Journal of Organic Chemistry Vol. 79 Iss. 11 (2014) p. 5334 - 5337
Available at: http://works.bepress.com/arthur_winter/4/