Abstract
The synthesis of 3‐(1′,1′‐difluoroalkyl)‐3‐hydroxyindolin‐2‐ones by employing α,α‐difluoro‐α‐phenylsulfanyl‐α‐trimethylsilylmethane (PhSCF2SiMe3) as a gem‐difluoromethylene building block is described. The reaction involves a fluoride‐catalyzed nucleophilic addition of PhSCF2SiMe3 to various isatin derivatives followed by the reductive cleavage of the phenylsulfanyl group to lead to 3‐(difluoromethyl)‐3‐hydroxyindolin‐2‐ones in good yields. Under similar reduction conditions but in the presence of activated olefins, an intermolecular radical trapping reaction took place to yield 3‐(1′,1′‐difluoroalkyl)‐3‐hydroxyindolin‐2‐one derivatives.
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