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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 597673Generated: October 30, 2026

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

https://huagongshe.com/reaction/597673

Reaction equation

Participants

RoleNameHCIDCharge
ReactantL-PhenylalanineHCID 6140—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 13305521HCID 13305521—
SolventWaterHCID 962—
Solventtert-ButanolHCID 6386—
Product(2S)-2-[(4-methoxyphenyl)methoxycarbonylamino]-3-phenylpropanoic acidHCID 1182366662.3%

Reaction Steps

L-Phenylalanine (330 mg.) and sodium bicarbonate (202 mg.) were dissolved in water (10 ml.) under heating and allowed to stand. A solution of diethyl 2-(4-methoxybenzyloxycarbonyloxyimino)malonate (1.0 g.) in tert-butyl alcohol (10 ml.) was added to the solution with stirring at room temperature and water (10 ml.) was added thereto, the mixture was then stirred for 2 hours at room temperature. The reaction mixture was brought to pH 9 by adding water (20 ml.) and saturated sodium bicarbonate aqueous solution (10 ml.), and water (10 ml.) was added thereto. The resulting mixture was then washed twice with ethyl acetate (20 ml.). The aqueous layer was adjusted to pH 7 with a 10% citric acid aqueous solution, washed twice with ethyl acetate (30 ml.), adjusted to pH 3.5 with a 10% citric acid aqueous solution and extracted three times with ethyl acetate (30 ml.). The extract was washed with a sodium chloride aqueous solution and dried over magnesium sulfate. The solvent was distilled off under reduced pressure to give N-(4-methoxybenzyloxycarbonyl)-L-phenyalanine (410 mg.), oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04014915
Source datasetuspto-grants-1977_03
ORD IDord-6ed214ce0a1a4aae8ee07c52a9aac82b
Source noteuspto-grants-1977_03