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


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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.

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G. Chernysheva

Favorskii Irkutsk Institute of Chemistry, Siberian Branch

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Email: gelya2010@irioch.irk.ru
俄罗斯联邦, ul. Favorskogo 1, Irkutsk, 664033

I. Nikitin

Favorskii Irkutsk Institute of Chemistry, Siberian Branch

Email: gelya2010@irioch.irk.ru
俄罗斯联邦, ul. Favorskogo 1, Irkutsk, 664033

I. Rozentsveig

Favorskii Irkutsk Institute of Chemistry, Siberian Branch

Email: gelya2010@irioch.irk.ru
俄罗斯联邦, ul. Favorskogo 1, Irkutsk, 664033

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