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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2230813Generated: October 29, 2026

Water → L-Phenylalanine, methyl ester

https://huagongshe.com/reaction/2230813

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantHCID 12042588HCID 12042588—
ReactantPropan-2-one--dichloromethane (1/1)HCID 21584124—
CatalystZincHCID 23994—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
SolventAmmonium ChlorideHCID 25517—
ProductL-Phenylalanine, methyl esterHCID 736234207.3%

Reaction Steps

To a suspension of N-[[1-[2-(acetylamino)ethyl]cyclopentyl]thioxomethyl]-4-nitro-L-phenylalanine methyl ester (740 mg, 1.75 mmol), zinc dust (1.14 g, 17.5 mmol) and ammonium chloride (1.41 g, 26.3 mmol) in methanol (20 mL) was added H2O (10 mL) slowly over 5 min. After stirring for 20 min, the reaction mixture was diluted with ethyl acetate (80 mL) and sat. ammonium chloride solution (25 mL). The separated aqueous layer was back-extracted with ethyl acetate (3×25 mL) and the organic layers were combined, dried over Na2SO4, filtered and concentrated in vacuo. The residual oil was dried under high vacuum for 2 h to give the crude amine (750 mg) which was by flash silica gel column chromatography (dichloromethane-acetone 2:1) to furnish 4-amino-N-[[1-[2-acetylamino)ethyl]cyclopentyl]thioxomethyl]-L-phenylalanine methyl ester (650 mg, 95%). HR MS: Obs. mass, 392.2016. Calcd. mass, 392.2008 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06426348B1
Source datasetuspto-grants-2002_07
ORD IDord-60a01de332ea49649b3c7a31f5a5f8a8
Source noteuspto-grants-2002_07