Issue 110, 2015

A solvent- and catalyst-free domino reaction for the efficient synthesis of 3-arylthiazolidine-2-thiones under microwave irradiation

Abstract

A facile synthesis of 4-hydroxy-3-arylthiazolidine-2-thiones through novel domino reactions of aryl isothiocyanates and 1,4-dithiane-2,5-diol under solvent- and catalyst-free microwave irradiation is reported. This highly atom efficient reaction presumably proceeds via 2-mercaptoacetaldehyde generation/thia-Michael addition/regioselective hemiaminalization domino sequence. This reaction also proceeds in good yields with aryl isocyanates affording 3-phenylthiazol-2(3H)-ones.

Graphical abstract: A solvent- and catalyst-free domino reaction for the efficient synthesis of 3-arylthiazolidine-2-thiones under microwave irradiation

Supplementary files

Article information

Article type
Paper
Submitted
16 Sep 2015
Accepted
15 Oct 2015
First published
16 Oct 2015

RSC Adv., 2015,5, 90451-90456

Author version available

A solvent- and catalyst-free domino reaction for the efficient synthesis of 3-arylthiazolidine-2-thiones under microwave irradiation

S. V. Kumar, S. Muthusubramanian and S. Perumal, RSC Adv., 2015, 5, 90451 DOI: 10.1039/C5RA19112B

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