Ma
et al. have reported the efficient [3 + 2] cycloaddition reactions of arynes with CF
3CHN
2 for the synthesis of 3-trifluoromethyl-1
H-indazoles. According to their results, arynes
in situ generated from 2-(trimethylsilyl)phenyl triflate by treatment with
CsF react with CF
3CHN
2 in the presence of
TEBAC under mild conditions to afford the corresponding 3-trifluoromethyl-1
H-indazole derivatives in high yields. Since 3-trifluoromethylindazoles are useful because of their potential biological activities, this reaction is expected to be an experimentally simple synthetic method for those compounds.