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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49524Generated: October 25, 2026

Triethylamine → 5-Formyl-2-methoxy-N-[[4-(trifluoromethyl)phenyl]methyl]-benzamide

https://huagongshe.com/reaction/49524

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
Reactant4-(Trifluoromethyl)benzylamineHCID 76804—
Reactant5-Formyl-2-methoxybenzoic acidHCID 3926683—
SolventDichloromethaneHCID 6344—
Product5-Formyl-2-methoxy-N-[[4-(trifluoromethyl)phenyl]methyl]-benzamideHCID 1209466178%

Reaction Steps

To a suspension of 1.00 g of 5-formyl-2-methoxybenzoic acid in 50 ml of methylene chloride were added 1.00 ml of triethylamine and 0.60 ml of ethyl chlorocarbonate, and the mixture was stirred for 15 minutes at room temperature. Then, a solution of 1.17 g of 4-trifluoromethylbenzylamine in 10 ml of methylene chloride was added and the mixture was stirred further for 3 hours at room temperature. After washed with water, the reaction mixture was dried over anhydrous sodium sulfate and the solvent was distilled off under reduced pressure. The residue obtained was purified by means of column chromatography (silica gel, hexane:ethyl acetate=1:1) and then recrystallized from a mixed solvent of diethyl ether-ethyl acetate-hexane to obtain 1.46 g of 5-formyl-2-methoxy-N-(4-trifluoromethylbenzyl)benzamide as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06706763B1
Source datasetuspto-grants-2004_03
ORD IDord-85c9d352781a4a668ba10aa38b2d8687
Source noteuspto-grants-2004_03