Radical reaction produces novel fluoroalkyl compounds in a versatile approach, highlighting hydrolysis potential.
The radical reaction of aryl-substituted vinyl cyclohexafluoropropane-1,3-bis(sulfonyl)amides (c-HFSI) followed by hydrolysis affords novel fluoroalkyl compounds. The key process in this reaction is the radical addition of c-HFSI to vinyl triflate, which is followed by β-cleavage (ring-opening reaction) and subsequent sulfur dioxide elimination to form fluoroalkyl radicals. By replacement of the hydrolysis with a reduction reaction, a robust polymer was obtained.
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Terauchi et al. (2025) studied this question.
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