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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2186784Generated: October 26, 2026

o-Benzylbenzoic acid → 2-Benzyl-N-(3,5-bis-trifluoromethyl-benzyl)-benzamide

https://huagongshe.com/reaction/2186784

Reaction equation

Participants

RoleNameHCIDCharge
Reactanto-Benzylbenzoic acidHCID 11924—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant3,5-Bis(trifluoromethyl)benzylamineHCID 521099—
SolventTetrahydrofuranHCID 8028—
Product2-Benzyl-N-(3,5-bis-trifluoromethyl-benzyl)-benzamideHCID 982437349%

Reaction Steps

To a solution of 255 mg (1.2 mmol) 2-benzylbenzoic acid in 1.5 ml tetrahydrofuran at 0° C. were added 195 mg (1.2 mmol) 1,1′-carbonyldiimidazole. After stirring for 2.5 h at room temperature, a solution of 243 mg (1.0 mmol) 3,5 bis(trifluoromethyl)benzylamine in 0.5 ml tetrahydrofuran was added and stirring was continued overnight. The solvent was removed in vacuo and the residue was purified by flash chromatography to give 210 mg (49%) of the title compound as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06407111B1
Source datasetuspto-grants-2002_06
ORD IDord-caf8671f44e4452797a0d35236aceaf0
Source noteuspto-grants-2002_06