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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1256952Generated: November 1, 2026

4-(Trifluoromethoxy)benzoyl Chloride → N-[2-(5-Chloro-2H-benzotriazol-2-yl)-1-cyano-1-methylethyl]-4-trifluoromethoxybenzamide

https://huagongshe.com/reaction/1256952

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Trifluoromethoxy)benzoyl ChlorideHCID 142110—
Reactant2-amino-3-(5-chloro-2H-benzotriazol-2-yl)-2-methylpropionitrileHCID 66620045—
SolventDichloromethaneHCID 6344—
ProductN-[2-(5-Chloro-2H-benzotriazol-2-yl)-1-cyano-1-methylethyl]-4-trifluoromethoxybenzamideHCID 2512156655.6%

Reaction Steps

4-trifluoromethoxybenzoyl chloride (0.34 g) was added to a solution of 2-amino-3-(5-chloro-2H-benzotriazol-2-yl)-2-methylpropionitrile (0.3 g) in dry DCM mixed with TEA (0.27 mL). The reaction mixture was stirred 48 hours at room temperature. Silica gel was added to the reaction mixture and solvent evaporated under reduced pressure. The resulting crude product loaded on silica gel was purified by chromatography (SiO2, heptane/EA) to afford the title compound as a white solid (0.3 g, 54%). Rf=0.7 (1:1 EA/heptane). MS (ES): M/Z [M+H]=424. 1H NMR: (400 MHz, DMSO-d6): 1.74 (s, 3H), 5.39-5.49 (m, 2H), 7.48 (dd, J=9.1, 1.9 Hz, 1H), 7.51 (br d, J=8.0 Hz, 2H), 7.93 (m, 2H), 8.01 (dd, J=9.1, 0.6 Hz, 1H), 8.13 (dd, J=1.9, 0.6 Hz, 1H) and 8.92 (s, 1H). 19F NMR (376 MHz, DMSO-d6): −57.09 (s, 3F).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461176B2
Source datasetuspto-grants-2013_06
ORD IDord-dfd158c2e2d34692944d4ec39192df39
Source noteuspto-grants-2013_06