Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 393779Generated: October 25, 2026

1-Phenethylamine → N-((1R)-1-Phenylethyl)glycine ethyl ester

https://huagongshe.com/reaction/393779

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-PhenethylamineHCID 7408—
ReactantEthyl bromoacetateHCID 7748—
ReactantDiisopropylethylamineHCID 81531—
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 numberUS06809105B2
Source datasetuspto-grants-2004_10
ORD IDord-874c05c4067740ca9321c982f398fa0b
Source noteuspto-grants-2004_10