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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1358612Generated: October 26, 2026

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

https://huagongshe.com/reaction/1358612

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 numberUS06596773B2
Source datasetuspto-grants-2003_07
ORD IDord-d1857aea3757476a9b3976ae0995923a
Source noteuspto-grants-2003_07