Abstract
The alkylation of the p-toluenesulfinate anion in methanol or dimethylformamide by methyl iodide, methyl sulfate, and methyl p-toluenesulfonate gives both methyl p-toluenesulfinate and methyl p-tolyl sulfone. Alkylation of the ambident anion with hard alkylating agents gives predominantly the ester, whereas a soft alkylating agent gives predominantly the sulfone. © 1968, American Chemical Society. All rights reserved.
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CITATION STYLE
APA
Meek, J. S., & Fowler, J. S. (1968). O and S methylation of the ambident p-toluenesulfinate anion. Journal of Organic Chemistry, 33(9), 3422–3424. https://doi.org/10.1021/jo01273a014
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