Synlett 2013; 24(6): 775-776
DOI: 10.1055/s-0032-1317796
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© Georg Thieme Verlag Stuttgart · New York

Mercaptoacetic Acid

Eliza de Lucas Chazin
Laboratório HETBIO - Instituto de Química Universidade Federal Fluminense, UFF, CEP: 24020-141, Niterói, Rio de Janeiro, Brazil   Email: elizachazin@gmail.com
› Author Affiliations
Further Information

Publication History

Publication Date:
08 March 2013 (online)

Introduction

Mercaptoacetic acid (3), also known as thioglycolic acid, is a liquid miscible with water and with most organic solvents such as alcohols, ether, chloroform and benzene.[ 1 ] It is widely described in the literature, especially as a substrate for the synthesis of pharmacologically active heterocycles[ 2 ] including 1,3-thiazolidin-4-ones,[ 3 ] 1,4-thiazepines[ 4 ] and thiazoles.[ 5 ] It is also used for the formation of spiro derivatives,[ 6 ] in multicomponent reactions, and in removing the nosyl protecting group from amine functions of α-amino acids.[ 7 ]

 
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