Journal
MONATSHEFTE FUR CHEMIE
Volume 138, Issue 9, Pages 871-873Publisher
SPRINGER WIEN
DOI: 10.1007/s00706-007-0685-3
Keywords
ethylenebis(N-methylimidazolium)chlorochromate; oxidation; thiols; sulfides
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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.
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