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DOI: 10.1055/s-2006-950353
Sulfonyl Chloride Formation from Thiol Derivatives by N-Chlorosuccinimide Mediated Oxidation
Publication History
Publication Date:
02 November 2006 (online)
Abstract
Oxidation of several thiol derivatives by a combination of N-chlorosuccinimide and dilute hydrochloric acid proceeded smoothly, affording the corresponding sulfonyl chlorides in good yield.
Key words
thiol derivatives - oxidation - solvent effects - NCS - chlorosulfonation
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11a The yields of 2i, 2a from 1i, 4a and 4c (Tables 2 and 4):
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References
Oxidation of 3e with 5; the procedure was the same as the general procedure for NCS. This reaction required 2 equiv of 5.
14Oxidation of 3e with 6; the procedure was the same as the general procedure for NCS. This reaction required 1.3 equiv of 6. The resulting solid was filtered off and washed with IPE (3.5 v/w to NCS) before work-up.
15Depending on the substrate properties, e.g. solubility, reactivity may somewhat differ from these results. Especially for large-scale synthesis, appropriate hazardous safety evaluations should be undertaken.