1-Chloroethenesulfonyl chloride is a reagent that can just with little heating yield acetylene. It is bench-stable oil, soluble in all common aprotic organic solvents. Usually, the reagent is applied for 1,3 -dipolar cycloaddition, which can be performed without solvent, just the substrate in the 1-chloroethenesulfonyl chloride as solvent and reagent1. After the reaction, the product is easily separated from the reagent by chromatography.
Synonyms: 1-chloroethenesulfonyl chloride; 1-chloro-1-ethenesulfonyl chloride; 1-chloroethylenesulfonyl chloride
Identification of 4-Substituted 1,2,3-Triazoles as Novel Oxazolidinone Antibacterial Agents with Reduced Activity against Monoamine Oxidase A.
Reck F.; Zhou F.; Girardot M.; Kern G.; Eyermann C.; Hales N.; Ramsay R.; Gravestock M. J Med Chem 2005, 48 (2), 499–506. DOI: 10.1021/jm0400810
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