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. 2022 Oct 17;13(44):12971–12979. doi: 10.1039/d2sc03879j

Stoichiometric C–H bond pentafluoroethylation by 1a.

Entry Substrate Conditions Yield [%]
1 graphic file with name d2sc03879j-u1.jpg 0
2 graphic file with name d2sc03879j-u2.jpg K2S2O8 (1 equiv.) 75
3 graphic file with name d2sc03879j-u3.jpg K2S2O8 (1 equiv.) 80
4 graphic file with name d2sc03879j-u4.jpg K2S2O8 (1 equiv.) 38
5 graphic file with name d2sc03879j-u5.jpg K2S2O8 (1 equiv.) 50
6 graphic file with name d2sc03879j-u6.jpg K2S2O8 (1 equiv.) 37
a

Reactions were performed for 24 hours using 1 equiv. of the substrate, and 1 equiv. of 1 in DMSO at RT under N2 unless indicated otherwise. The yields were determined by 19F NMR based on integration against α,α,α-trifluorotoluene as an internal standard.