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. 2022 Jan 5;13(8):2270–2279. doi: 10.1039/d1sc06267k

Scheme 5. Synthesis of triflamides by reaction of CF3SO2F with amines and azoles. Reaction was carried out on 1.0 mmol scale and reported yields are after column chromatography unless noted otherwise. Between brackets is given the 19F NMR yield using PhCF3 as internal standard, between parentheses the reaction time. [a] Isolated yield of pure material after aqueous work-up. [b] 3.0 equiv. of base was used. [c] 2.5 equiv. of CF3SO2F gas was used. [d] 3.5 equiv. of base was used. [e] 2.0 equiv. of CF3SO2F was generated. [f] K2CO3 was used as the base. [g] 2.5 equiv. of base was used.

Scheme 5