Journal of Sulfur Chemistry · 2012 · 21 citations · 21 references
Natural SciencesChemistryCatalysisOrganic ChemistryReaction EngineeringHeterocyclic ChemistryOrganic SynthesisSolvent-free SynthesisCarbon DisulfideDisulfide ChemistryMild Reaction Conditions
Abstract A simple and efficient one-pot synthesis of 1-[3-alkyl-4-methyl-2-thioxo-2,3-dihydrothiazole-5-yl]-ethanones from the reaction of primary alkylamines and carbon disulfide in the presence of 3-chloro acetylacetone is described. This protocol has several advantages such as lack of need for a solvent and catalyst, high yields, mild conditions and short reaction times. Keywords: 3-chloro acetylacetone2-thioxo-2,3-dihydrothiazolecarbon disulfideprimary alkylaminesmulticomponent reaction Acknowledgements We are thankful to the Gachsaran branch, Islamic Azad University, for the partial support of this work.
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