An　effective　protocol　for　the　difluoromethylation　of　tosylhydrazone　compounds　under　mild　conditions　is　disclosed　via　a　transition-metal-free　pathway;　ClCF2H　is　almost　quantitatively　converted　under　the　set　conditions.　In　this　transformation,　the　process　in　which　tosylhydrazones　are　decomposed　to　lead　to　diazo　species　has　been　completely　suppressed.　This　transformation　enables　tosylhydrazones　as　efficient　difluorocarbene　scavengers　and　the　corresponding　difluoromethylated　products　were　obtained　in　good　yields　with　high　functional-group　tolerance.