Abstract
The synthesis of phenacyl-bis(dithiocarbamates) has been reported by metal-free trifunctionalization of phenylacetylene systems by following a one-pot two-step strategy. Phenyl acetylene undergoes molecular bromine-mediated oxidative bromination followed by nucleophilic substitution with the freshly prepared dithiocarbamate salt which is prepared by the prompt reaction of amine and CS2 in the presence of triethylamine base. A series of gem-bis(dithiocarbamates) are prepared using various secondary amines and phenylacetylene systems containing different substituents.
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