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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1252188Generated: November 1, 2026

Ethyl 2-bromopropionate → HCID 20141170, compound

https://huagongshe.com/reaction/1252188

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-bromopropionateHCID 79040—
Reactant2-BromobenzaldehydeHCID 81129—
ReactantPotassium tert-butoxideHCID 23665647—
ProductHCID 20141170HCID 2014117069%

Reaction Steps

A 50 g (0.27 mole) sample of 2-bromobenzaldehyde was added to 33.3 g of dry potassium t-butoxide under N2 at -78°. A 48.9 g (0.27 mole) sample of ethyl 2-bromopropionate was added slowly with stirring. The mixture was allowed to warm to room temperature and stir for 18 hr. The mixture was partitioned between ether and dilute HCl. The ether was washed with brine, dried (MgSO4) and the solvent evaporated in vacuo. The residue was distilled under vacuum to give 53.2 g (69% yield) of ethyl 3-(2-bromophenyl)-2-methyloxiraneacetate as an oil, bp 110°-120° C., 0.005 mm/Hg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04742084
Source datasetuspto-grants-1988_05
ORD IDord-815fce3a7fd44e7bb429575478c6e866
Source noteuspto-grants-1988_05