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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2251420Generated: October 26, 2026

Ethyl bromoacetate → N-((1R)-1-Phenylethyl)glycine ethyl ester

https://huagongshe.com/reaction/2251420

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantDiisopropylethylamineHCID 81531—
Reactant1-Phenethylamine, (+)-HCID 643189—
SolventTolueneHCID 1140—
ProductN-((1R)-1-Phenylethyl)glycine ethyl esterHCID 645533363%

Reaction Steps

Ethyl bromoacetate (4.14 g; 24.8 mmol) was treated with (R)α-methylbenzylamine (3 g, 24.8 mmol) and ethyldiisopropylamine (3.2 g; 24.8 mmol) in toluene (100 mL). After heating at reflux for 18 hours, the mixture was cooled to room temperature and concentrated under reduced pressure. The residue was purified by flash chromatography (SiO2, 20% ethyl acetate/pentane) to provide the title compound (3.2 g, 63% yield). MS (DCI/NH3) m/z 208 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07319106B2
Source datasetuspto-grants-2008_01
ORD IDord-ea835f075e8642f397adc69f8d5a52c1
Source noteuspto-grants-2008_01