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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1918511Generated: November 2, 2026

Water → Ethyl 5-(bromomethyl)-1,2-oxazole-3-carboxylate

https://huagongshe.com/reaction/1918511

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPropargyl bromideHCID 7842—
ReactantSodium BicarbonateHCID 516892—
ReactantEthyl chloro(hydroximino)acetateHCID 6816376—
SolventEthyl AcetateHCID 8857—
ProductEthyl 5-(bromomethyl)-1,2-oxazole-3-carboxylateHCID 1312495587.3%

Reaction Steps

A solution of ethyl 2-chloro-2-(hydroxyimino)acetate (11 g; 70.41 mmol) in ethyl acetate (60 mL) was added dropwise at room temperature to a mixture of 3-bromoprop-1-yne (15.2 mL; 141 mmol), sodium bicarbonate (11.95 g; 141 mmol), ethyl acetate (400 mL), and water (4 mL). The mixture was stirred at room temperature for 24 h and the solid was removed by filtration and washed with ethyl acetate. The filtrate was concentrated under reduced pressure and the residue was purified by flash chromatography on silica gel (eluent: 15 to 100% of dichloromethane in heptane) to give 14.38 g (87%) of ethyl 5-(bromomethyl)isoxazole-3-carboxylate as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618138B2
Source datasetuspto-grants-2013_12
ORD IDord-f9b9134b5e9d4b1e9c865a06f4d0d438
Source noteuspto-grants-2013_12