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Ethylenebis(N-methylimidazolium) Chlorochromate (EBMICC): An Efficient and Selective Reagent for the Oxidation of Thiols to Disulfides
Authors:Rahman Hosseinzadeh  Mahmood Tajbakhsh  Hamid Khaledi  Keivan Ghodrati
Affiliation:(1) Department of Chemistry, Mazandaran University, Babolsar, Iran
Abstract:Summary. Ethylenebis(N-methylimidazolium) chlorochromate was prepared by addition of N-methylimidazole to 1,2-dibromoethane to form the corresponding dibromide salt and subsequent treatment of this salt with CrO3 in 6N HCl solution. It is a stable yellow-orange solid, which oxidized thiols to the corresponding disulfides at room temperature. Selective oxidation of thiols in the presence of sulfides and hydroxyl groups was also achieved with this reagent.
Keywords:. Ethylenebis(N-methylimidazolium)chlorochromate   Oxidation   Thiols   Sulfides.
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