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January 1, 2019Chemical Communications90 citations

One-pot fluorosulfurylation of Grignard reagents using sulfuryl fluoride

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CLCayo LeeNBNicholas D. BallGSGlenn M. Sammis

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Abstract

Herein, we report a new method for the one-pot syntheses of sulfonyl fluorides. Addition of an alkyl, aryl, or heteroaryl Grignard to a solution of sulfuryl fluoride at ambient temperature affords the desired sulfonyl fluorides in 18-78% yield. Furthermore, this method is applicable for in situ sequential reactions, whereby the Grignard reagent can be converted to the corresponding diarylsulfone, sulfonate ester, or sulfonamide in a one-pot process.

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Lee et al. (2019) studied this question.

synapsesocial.com/papers/6a04ca2c684090886a2d32b9https://doi.org/10.1039/c9cc08487h
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