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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 458788Generated: October 30, 2026

Ethyl chloroformate → 3-(4-Benzyloxy-3-methoxy-phenyl)-propionamide

https://huagongshe.com/reaction/458788

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
ReactantAmmonium HydroxideHCID 14923—
Reactant3-(3-Methoxy-4-benzyloxyphenyl)propionic acidHCID 2752415—
SolventTetrahydrofuranHCID 8028—
Product3-(4-Benzyloxy-3-methoxy-phenyl)-propionamideHCID 18442581100%

Reaction Conditions

Temperature-15 °C

Reaction Steps

To a stirred solution of 3-(4-benzyloxy-3-methoxy-phenyl)-propionic acid (8.38 g, 29.30 mmol) in dry THF (110 ml), under nitrogen, was added TEA (4.5 ml, 32.33 mmol), and the resulting mixture was cooled to −10° C. before ethyl chloroformate (3.1 ml, 32.53 mmol) was added dropwise. After stirring at −10° C. (20 min), ammonium hydroxide (25% in water, 65 ml) in THF (65 ml) was added and the mixture was stirred at −15° C. for 30 min and then at RT for 1.5 h. The reaction mixture was concentrated in vacuo, extracted three times with CH2Cl2 and the combined organic extracts were washed with saturated aqueous NaHCO3 and brine. The organic phase was dried over anhydrous MgSO4, filtered and concentrated to give the title compound (8.40 g, 29.30 mmol, 100%) as a colorless solid. No further purification of the crude amide was necessary.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07192950B2
Source datasetuspto-grants-2007_03
ORD IDord-4b87c93c90e7498ea6fef75bd7789d22
Source noteuspto-grants-2007_03