Sulfonamidation of halogen-substituted electrophiles with N-(2,2,2-trichloroethyl)arenesulfonamides


Cite item

Full Text

Open Access Open Access
Restricted Access Access granted
Restricted Access Subscription Access

Abstract

Reactions of N-(2,2,2-trichloroethyl)arenesulfonamides with primary alkyl bromides and iodides, allyl bromide, chloroacetonitrile, and benzyl chloride in acetonitrile on heating in the presence of potassium carbonate gave the corresponding N-alkyl-N-(2,2,2-trichloroethyl)arenesulfonamides.

About the authors

G. N. Chernysheva

Favorskii Irkutsk Institute of Chemistry, Siberian Branch

Author for correspondence.
Email: gelya2010@irioch.irk.ru
Russian Federation, ul. Favorskogo 1, Irkutsk, 664033

I. V. Nikitin

Favorskii Irkutsk Institute of Chemistry, Siberian Branch

Email: gelya2010@irioch.irk.ru
Russian Federation, ul. Favorskogo 1, Irkutsk, 664033

I. B. Rozentsveig

Favorskii Irkutsk Institute of Chemistry, Siberian Branch

Email: gelya2010@irioch.irk.ru
Russian Federation, ul. Favorskogo 1, Irkutsk, 664033

Supplementary files

Supplementary Files
Action
1. JATS XML

Copyright (c) 2017 Pleiades Publishing, Ltd.