p-Toluenesulfonic Acid–Celite as a Reagent for Synthesis of Esters of Alkylphosphonic Acids under Solvent-Free Conditions-Reference-Cited by-同舟云学术

p-Toluenesulfonic Acid–Celite as a Reagent for Synthesis of Esters of Alkylphosphonic Acids under Solvent-Free Conditions

Published:2007-06 Issue:6 Volume:2007 Page:328-331
ISSN:1747-5198
Container-title:Journal of Chemical Research
language:en
Short-container-title:Journal of Chemical Research

Author:

Gupta Arvind K.¹,Kumar Rajesh¹,Dubey Devendra K.¹,Kaushik M.P.¹

Affiliation:

1. Defence Research and Development Establishment, Jhansi Road, Gwalior-47400Z, India

Abstract

The coupling reaction of alkylphosphonic acids and alcohols on the surface of p-toluenesulfonic acid–Celite under mild and solvent-free conditions gave the corresponding phosphonates in excellent yields. This method provides a useful rapid synthesis of phosphonates for use in the unambiguous identification of chemical warfare agents.

Publisher

SAGE Publications

Subject

General Chemistry

Link

http://journals.sagepub.com/doi/pdf/10.3184/030823407X218066

Reference35 articles.

1. (a) PapazoglouE.S., In Handbook of Building Materials for Fire Protection vol. 88, pp. 1-4 HarperC.A., Ed: McGraw-Hill: New York. 2004

2. John Wiley: New York, 1993, pp. 976-998.

3. (a) PapazoglouE.S., In Handbook of Building Materials for Fire Protection vol. 88, pp. 1-4 HarperC.A., Ed: McGraw-Hill: New York. 2004;

4. (b) E.D. Weil, Phosphorus Flame Retardents. In Kirk-Othmer Encyclopedia of Chemical Technology, vol. 10 4th edn.; John Wiley: New York, 1993, pp. 976-998.

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