Metal-Free Amidation Reactions of Terminal Alkynes with Benzenesulfonamide
Sachinta Mahato1, Sougata Santra2, Grigory V Zyryanov2,3
1Department of Chemistry , Visva-Bharati (A Central University) , Santiniketan 731235 , India.
Abstract:
A novel and efficient approach has been developed to synthesize α-sulfonylamino ketones through the reaction between terminal alkynes and sulfonamides under ambient air using PIDA (diacetoxy iodobenzene). A library of α-sulfonylamino ketone derivatives having a variety of substituents has been synthesized. A plausible reaction pathway has been predicted. This reaction offers a broad substrate scope, metal-free synthesis, excellent regioselectivity, easily accessible reactants, and room temperature reaction conditions under ambient air and is operationally simple. A gram-scale synthesis demonstrates the potential applications of the present method. In addition, we have also synthesized α-acetoxy ketones in the case of absence of sulfonamide.
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Table 1: Properties of the alkali metals
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