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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1720506Generated: November 3, 2026

Benzenepropanoic acid → N-(3-phenylpropionyl)-L-proline benzyl ester

https://huagongshe.com/reaction/1720506

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenepropanoic acidHCID 107—
ReactantTriethylamineHCID 8471—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantProline benzyl ester hydrochlorideHCID 2733413—
SolventDichloromethaneHCID 6344—
ProductN-(3-phenylpropionyl)-L-proline benzyl esterHCID 4513942393.5%

Reaction Steps

To a solution of L-proline benzyl ester hydrochloride (20.0 g) in methylene chloride (250 ml) were added triethylamine (11.5 ml), 3-phenylpropionic acid (13.7 g) and DCC (18.8 g) under ice-cooling, and the mixture was stirred for 2 hours. After stirring at room temperature for 14 hours, the insoluble material was filtered off, and the filtrate was concentrated. The residue was dissolved in ethyl acetate, and the solution was washed with 1N hydrochloric acid, saturated aqueous solution of sodium bicarbonate and saturated brine, dried over anhydrous magnesium sulfate, and concentrated. The residue was purified by silica gel column chromatography (eluate: hexane-ethyl acetate). To thus-obtained N-(3-phenylpropionyl)-L-proline benzyl ester (26.1 g) in 1% water-containing methanol (200 ml) was added 10% Pd--C (3.0 g), and the mixture was stirred at room temperature under hydrogen atmosphere for 2.5 hours. The catalyst was filtered off, and the filtrate was concentrated to give 17.4 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05506256
Source datasetuspto-grants-1996_04
ORD IDord-9036e7c8033c48ff811aedeed9fb48eb
Source noteuspto-grants-1996_04