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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1826086Generated: November 1, 2026

Triethylamine → Ethyl 2-[4-methoxy-3-({[4-(trifluoromethyl)benzoyl]amino}methyl)benzyl]butanoate

https://huagongshe.com/reaction/1826086

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-(Trifluoromethyl)benzoic acidHCID 9966—
ReactantEthyl chloroformateHCID 10928—
ReactantEthyl 2-[(3-aminomethyl-4-methoxyphenyl)-methyl]butyrate hydrochlorideHCID 22139981—
SolventDichloromethaneHCID 6344—
ProductEthyl 2-[4-methoxy-3-({[4-(trifluoromethyl)benzoyl]amino}methyl)benzyl]butanoateHCID 1100463393.3%

Reaction Steps

To a solution of 4-(trifluoromethyl)benzoic acid (114 mg, 0.600 mmol) and triethylamine (0.21 mL, 1.51 mmol) in dichloromethane (3 mL), ethyl chlorocarbonate (0.063 mL, 0.659 mmol) was added under stirring and cooling with ice, and the mixture was stirred for 20 minutes. Next, after ethyl 2-ethyl-3-[3-(aminomethyl)-4-methoxyphenyl]propanoate hydrochloride (200 mg, 0.663 mmol) was added, the mixture was stirred for 1 hour under cooling with ice and for 3 hours at room temperature. Dichloromethane (20 mL) was added to the reaction mixture, which was washed with 1 mol/L hydrochloric acid, saturated aqueous solution of sodium hydrogencarbonate and brine, dried over anhydrous sodium sulfate, and then concentrated. The residue was purified by silica gel column chromatography (eluent: n-hexane:ethyl acetate=4:1 v/v) to afford 245 mg (93%) of the title compound as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07049342B2
Source datasetuspto-grants-2006_05
ORD IDord-a4c6184cdd674d08b7da1aa97b5c970f
Source noteuspto-grants-2006_05