Issue 31, 2023

Base-mediated synthesis of cyclic dithiocarbamates from 1-amino-3-chloropropan-2-ol derivatives and carbon disulfide

Abstract

An efficient method for the preparation of six-membered cyclic dithiocarbamates is described, in which triethylamine effectively promotes the reaction of 1-amino-3-chloropropan-2-ol derivatives with carbon disulfide. On the basis of the experimental and theoretical studies, a reaction mechanism is proposed to explain the difference between the present reaction and our previously reported carbon dioxide fixation.

Graphical abstract: Base-mediated synthesis of cyclic dithiocarbamates from 1-amino-3-chloropropan-2-ol derivatives and carbon disulfide

Supplementary files

Article information

Article type
Communication
Submitted
05 Jul 2023
Accepted
18 Jul 2023
First published
18 Jul 2023

Org. Biomol. Chem., 2023,21, 6293-6297

Base-mediated synthesis of cyclic dithiocarbamates from 1-amino-3-chloropropan-2-ol derivatives and carbon disulfide

Y. Toda, M. Iwasaki and H. Suga, Org. Biomol. Chem., 2023, 21, 6293 DOI: 10.1039/D3OB01070H

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