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Photoredox-Catalyzed Preparation of Sulfones Using Bis-Piperidine Sulfur Dioxide - An Underutilized Reagent for SO 2 Transfer.

Oliver M GriffithsHenrique A EstevesDarcy C EmmetSteven V Ley
Published in: Chemistry (Weinheim an der Bergstrasse, Germany) (2024)
Sulfonyl groups are widely observed in biologically relevant molecules and consequently, SO 2 capture is an increasingly attractive method to prepare these sulfonyl-containing compounds given the range of SO 2 -surrogates now available as alternatives to using the neat gas. This, along with the advent of photoredox catalysis, has enabled mild radical capture of SO 2 to emerge as an effective route to sulfonyl compounds. Here we report a photoredox-catalyzed cross-electrophile sulfonylation of aryl and alkyl bromides making use of a previously under-used amine-SO 2 surrogate; bis(piperidine) sulfur dioxide (PIPSO). A broad selection of alkyl and aryl bromides were photocatalytically converted to their corresponding sulfinates and then trapped with various electrophiles in a one-pot multistep procedure to prepare sulfones and sulfonamides.
Keyphrases
  • visible light
  • room temperature
  • ionic liquid
  • minimally invasive
  • molecularly imprinted
  • high resolution
  • mass spectrometry
  • tandem mass spectrometry