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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 872944Generated: October 30, 2026

Triethylamine → Ethyl 3-(4-fluorophenyl)-5-methyl-1,2-oxazole-4-carboxylate

https://huagongshe.com/reaction/872944

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl 2-butynoateHCID 78043—
Reactant4-Fluoro-N-hydroxybenzimidoyl chlorideHCID 5706360—
SolventDiethyl EtherHCID 3283—
ProductEthyl 3-(4-fluorophenyl)-5-methyl-1,2-oxazole-4-carboxylateHCID 2230906161.4%

Reaction Steps

To a solution of (E)- and/or (Z)—N-hydroxy-4-fluoro-benzenecarboximidoyl chloride (15.4 g, 89 mmol) (11.1 g, 64 mmol) in diethylether (151 mL) was added ethyl 2-butynoate (7.2 g, 7.5 mL, 64 mmol) at 0° C. followed by the dropwise addition of triethylamine (7.8 g, 10.7 mL, 77 mmol) and the resulting mixture allowed to warm up to room temperature overnight. The mixture was then poured onto ice-water, and extracted with diethylether. The combined organic layers were then washed with water and brine, dried over sodium sulfate and evaporated. Purification by chromatography (SiO2, heptane:ethyl acetate=100:0 to 1:1) afforded the title compound (9.8 g, 44%) which was obtained as an off white solid. MS: m/e=250.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08975397B2
Source datasetuspto-grants-2015_03
ORD IDord-5d3a3acfa5d54554853c591517058010
Source noteuspto-grants-2015_03