Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 276926Generated: October 25, 2026

Benzyl chloroformate → Ethyl 3-{[(benzyloxy)carbonyl]amino}propanoate

https://huagongshe.com/reaction/276926

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
ReactantSodium HydroxideHCID 14798—
Reactantbeta-Alanine, ethyl ester, hydrochlorideHCID 458475—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 3-{[(benzyloxy)carbonyl]amino}propanoateHCID 12116647—

Reaction Conditions

Temperature2.5 °C

Reaction Steps

Ethyl 3-aminopropionate hydrochloride (10 g) was dissolved in a mixture of tetrahydrofuran (100 ml) and water, which was cooled at 0 to 5° C. in an ice bath and adjusted to pH 8.2 with 30% aqueous sodium hydroxide solution. To a resulting solution was added with care benzyloxycarbonyl chloride (10.3 ml), with maintaining the pH from pH 8.0 to 9.0 with 30% aqueous sodium hydroxide solution at 0 to 5° C. The reaction mixture was extracted with ethyl acetate (300 ml) and organic layer was separated, which was washed two times with saturated sodium chloride in water and dried over magnesium sulfate. Solvent was removed under reduced pressure to give ethyl 3-(benzyloxycarbonylamino)-propionate (15.3 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06355640B1
Source datasetuspto-grants-2002_03
ORD IDord-d98944a48c444e3782edaf7c9c5a6e29
Source noteuspto-grants-2002_03