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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 332303Generated: October 27, 2026

Triethylamine → Ethyl 3-(3-fluorophenyl)-5-methylisoxazole-4-carboxylate

https://huagongshe.com/reaction/332303

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl 2-butynoateHCID 78043—
Reactant3-fluoro-N-hydroxybenzene-1-carbonimidoyl chlorideHCID 14221338—
SolventDiethyl EtherHCID 3283—
ProductEthyl 3-(3-fluorophenyl)-5-methylisoxazole-4-carboxylateHCID 2230906039.5%

Reaction Steps

To a solution of (E)- and/or (Z)-N-hydroxy-3-fluoro-benzenecarboximidoyl chloride (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 (6.3 g, 39%) which was obtained as a white solid. MS: m/e=250.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08877783B2
Source datasetuspto-grants-2014_11
ORD IDord-ff0567269955498791ba32b1c8968aa7
Source noteuspto-grants-2014_11