Abstract
Abstract The acid-catalysed addition of trichloromethanesulphenyl chloride to 2,3-dihydrofuran yields 2-chloro-3-trichloromethylthiotetrahydrofuran. This is a useful intermediate for reactions with nucleophilic agents. The mechanism of the addition reaction is discussed and related to the behaviour of other sulphenyl chlorides toward the carbon-carbon double bond.
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