Abstract
Background: Although several methods are reported for the C-S bond formation, the microwave assisted method reported in this work is simple and proceeds with high yields in short time.
Methods: In the synthetic method, the targeted aryl sulfides were synthesized with the help of microwave by reacting halobenzenes, substituted thiophenols and potassium carbonate in the presence of dimethyl sulfoxide and water.
Results: All the aryl sulfides were obtained in good yield (87%-97%) with the help of microwave technique and in the presence of dimethyl sulfoxide: water as a solvent system.
Conclusion: Microwave assisted synthesis will be a useful alternative method for the synthesis of diverse range of aryl sulfides.
Keywords: Aqueous, catalyst, coupling, microwave, sulfides, thioethers.
Current Microwave Chemistry
Title:Catalyst Free Microwave Assisted Synthesis of Sulfides in Aqueous Media
Volume: 3 Issue: 3
Author(s): Sushilkumar S. Bahekar, Aniket P. Sarkate, Ishwari A. Kale and Pravin S. Wakte
Affiliation:
Keywords: Aqueous, catalyst, coupling, microwave, sulfides, thioethers.
Abstract: Background: Although several methods are reported for the C-S bond formation, the microwave assisted method reported in this work is simple and proceeds with high yields in short time.
Methods: In the synthetic method, the targeted aryl sulfides were synthesized with the help of microwave by reacting halobenzenes, substituted thiophenols and potassium carbonate in the presence of dimethyl sulfoxide and water.
Results: All the aryl sulfides were obtained in good yield (87%-97%) with the help of microwave technique and in the presence of dimethyl sulfoxide: water as a solvent system.
Conclusion: Microwave assisted synthesis will be a useful alternative method for the synthesis of diverse range of aryl sulfides.
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Cite this article as:
Bahekar S. Sushilkumar, Sarkate P. Aniket, Kale A. Ishwari and Wakte S. Pravin, Catalyst Free Microwave Assisted Synthesis of Sulfides in Aqueous Media, Current Microwave Chemistry 2016; 3 (3) . https://dx.doi.org/10.2174/2213335602666150930205918
DOI https://dx.doi.org/10.2174/2213335602666150930205918 |
Print ISSN 2213-3356 |
Publisher Name Bentham Science Publisher |
Online ISSN 2213-3364 |
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