Cyanuric Chloride: an Efficient Catalyst for Ring Opening of Epoxides with Thiols Under Solvent-Free Conditions

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doi:10.1071/CH07079

Cyanuric Chloride: an Efficient Catalyst for Ring Opening of Epoxides with Thiols Under Solvent-Free Conditions

Babasaheb P. Bandgar ^A ^B, Neeta S. Joshi ^A, Vinod T. Kamble ^A, Sanjay S. Sawant ^A

^A Organic Chemistry Research Laboratory, School of Chemical Sciences, Swami Ramanand Teerth Marathwada University, Nanded 431606, Maharashtra, India.
^B Corresponding author. Email: bandgar_bp@yahoo.com





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Australian Journal of Chemistry 61(3) 231–234 http://dx.doi.org/10.1071/CH07079
Submitted: 15 March 2007 Accepted: 6 February 2008 Published online: 26 March 2008

Abstract

2,4,6-Trichloro-1,3,5-triazine-catalyzed convenient and efficient ring opening of epoxides with thiols under solvent-free conditions is described. Short reaction time, mild reaction conditions, inexpensive and readily available catalyst, and excellent yields of products are attractive features of this methodology.