ORGANIC SYNTHESIS WITH SULPHONES - XVII. THE ANTI-MARKOWNIKOFF HALOSULPHONYLATION OF OLEFINS VIA AN IONIC PATHWAY, AND A NEW METHOD OF PREPARING BENZENESULPHONYL IODIDE

Article abstract of DOI:10.1016/0040-4020(80)80226-2

Iodine and bromine in the presence of sodium benzenesulphinate react with olefins in acetone solution to give halosulphones resulting from an apparent steric direction of attack at the intermediate halonium ion.A straightforward preparation of benzenesulphonyl iodide from benzenesulphonyl chloride and sodium iodide is also described.