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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1694640Generated: October 31, 2026

Triethylamine → Ethyl 5-[3-(trifluoromethyl)phenyl]-1,2-oxazole-3-carboxylate

https://huagongshe.com/reaction/1694640

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-Ethynyl-3-(trifluoromethyl)benzeneHCID 2778490—
ReactantEthyl 2-chloro-2-(hydroxyimino)acetateHCID 6399471—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 5-[3-(trifluoromethyl)phenyl]-1,2-oxazole-3-carboxylateHCID 53439058—

Reaction Steps

To a stirred solution of ethyl chlorooximidoacetate (6.68 g, 44.09 mmol) in tetrahydrofuran (90 mL) in an ice bath was added 3-(trifluoromethyl)phenylacetylene (5.0 g, 29.39 mmol) slowly, followed by triethylamine (8.19 mL, 58.78 mmol) dropwise. The resulting mixture was stirred at room temperature overnight, which was then filtered through a layer of silica gel (top) and anhydrous Na2SO4 (bottom), and washed with ethyl acetate. The filtrate was washed with water, the organic layer dried over sodium sulfate, and the solvent removed under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:Hexanes=1:9) to afford ethyl 5-[3-(trifluoromethyl)phenyl]isoxazole-3-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158810B2
Source datasetuspto-grants-2012_04
ORD IDord-7cd9aff82f6c4b5691c6a34e63a593b1
Source noteuspto-grants-2012_04