Abstract
An efficient one-pot method for the synthesis of organic disulfides from aryl and alkyl halides and potassium sulfide has been described. K2S acts as an inexpensive and readily available sulfur source. A variety of symmetric diaryl and dialkyl disulfides was prepared in good to excellent yields using NiCl2·6H2O and acetylacetone as the catalytic system.
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Financial support from Ilam university research council is gratefully acknowledged.
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Soleiman-Beigi, M., Arzehgar, Z. Symmetrical disulfide synthesis via nickel-catalysis using potassium sulfide as sulfur source. Monatsh Chem 147, 1759–1763 (2016). https://doi.org/10.1007/s00706-016-1673-2
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DOI: https://doi.org/10.1007/s00706-016-1673-2