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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 597676Generated: October 27, 2026

L-Phenylalanine → (2S)-2-[(4-methoxyphenyl)methoxycarbonylamino]-3-phenylpropanoic acid

https://huagongshe.com/reaction/597676

Reaction equation

Participants

RoleNameHCIDCharge
ReactantL-PhenylalanineHCID 6140—
ReactantTriethylamineHCID 8471—
Reactant1,4-DioxaneHCID 31275—
Reactant2-(4-Methoxybenzyloxycarbonyloxyimino)-2-phenylacetonitrileHCID 3916227—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product(2S)-2-[(4-methoxyphenyl)methoxycarbonylamino]-3-phenylpropanoic acidHCID 1182366664.7%

Reaction Steps

2-(4-Methoxybenzyl)oxycarbonyloxyimino-2-phenylacetonitrile (1.55 g.) was added to a solution of L-phenylalanine (826 mg.) and triethylamine (0.75 ml.) in a mixture of methanol (10 ml.), dioxane (1.5 ml.) and water (7.5 ml.) at room temperature the resulting mixture was stirred for 2 hours at room temperature. The reaction mixture was concentrated and benzene and a sodium bicarbonate aqueous solution were added to the residue. After shaking the resultant mixture, the aqueous layer was separated from the mixture, washed with ether, acidified with hydrochloric acid and extracted with ethyl acetate. The extract was washed with water, dried and concentrated. N-Hexane was added to the residue, and the precipitated crystals were collected by filtration and dried to give N-(4-methoxybenzyl)oxycarbonyl-L-phenylalanine (1.064 g.), mp 87° to 88° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04014915
Source datasetuspto-grants-1977_03
ORD IDord-dfb3965047144e62a4ddb4cd19cc9dee
Source noteuspto-grants-1977_03