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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2109845Generated: October 30, 2026

Ethyl bromoacetate → Methyl {2-[(benzyloxy)methyl]aziridin-1-yl}acetate

https://huagongshe.com/reaction/2109845

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-[(Benzyloxy)methyl]aziridineHCID 86602786—
SolventDichloromethaneHCID 6344—
ProductMethyl {2-[(benzyloxy)methyl]aziridin-1-yl}acetateHCID 57634653—

Reaction Steps

To a cold (−78° C.) solution of 2-[(benzyloxy)methyl]aziridine (0.42 g, 2.57 mmol) and N,N-diisopropylethylamine (0.5 mL, 2.90 mmol) in dichloromethane (15 mL) under an atmosphere of nitrogen, ethyl bromoacetate (0.39, 2.5 mmol) was added over a period of 1 h. The resultant mixture was allowed to slowly warm up to room temperature and stirred overnight. The resultant mixture was washed with brine, dried over anhydrous magnesium sulfate, filtered, and concentrated under vacuum. The residue was subjected to column chromatography on silica gel eluting with a mixture of 70% ethyl acetate in hexane. Collection and concentration of appropriate fractions provided the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07517532B2
Source datasetuspto-grants-2009_04
ORD IDord-05619cf4335748e0b8826f7da7a75642
Source noteuspto-grants-2009_04