Tetrabutylammonium Fluoride → 1-(2-Bromo-5-fluorophenyl)-1H-1,2,3-triazole

Participants

Reaction Conditions

Reaction Steps

1-(2-Bromo-5-fluorophenyl)-4-(trimethylsilyl)-1H-1,2,3-triazole (0.80 g, 2.55 mmol) was dissolved in tetrahydrofuran (10 mL) and tetrabutylammonium fluoride (2.8 mL, 2.80 mmol, 1.0 M in tetrahydrofuran) was added dropwise and the reaction mixture was stirred at 25° C. for 4 h. The resulting mixture was concentrated in vacuo and the residue was purified with a Biotage system on silica gel with hexanes:ethyl acetate (8:2 to 7:3) gradient as the eluent to afford the title compound as a white solid (0.36 g, 58% yield): 1H NMR (400 MHz, CDCl3) δ ppm: 8.06 (1 H, d, J=1.0 Hz), 7.90 (1 H, d, J=1.3 Hz), 7.76 (1 H, dd, J=8.8, 5.3 Hz), 7.39 (1 H, dd, J=8.3, 2.8 Hz), 7.19 (1 H, ddd, J=8.9, 7.5, 3.0 Hz), LCMS (+ESI, M+H+) m/z 242/244.

Provenance & Evidence