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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1695427Generated: November 1, 2026

Triethylamine → [3-(4-Fluoro-phenyl)-5-((E)-styryl)-isoxazol-4-yl]-methanol

https://huagongshe.com/reaction/1695427

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
ReactantSodium HydroxideHCID 14798—
ReactantSodium borohydrideHCID 4311764—
Reactant3-(4-Fluoro-phenyl)-5-((E)-styryl)-isoxazole-4-carboxylic acidHCID 66643836—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product[3-(4-Fluoro-phenyl)-5-((E)-styryl)-isoxazol-4-yl]-methanolHCID 6664390563%

Reaction Steps

To a solution of 3-(4-fluoro-phenyl)-5-((E)-styryl)-isoxazole-4-carboxylic acid (19.0 g, 61.4 mmol) and triethylamine (8.6 mL, 61.4 mmol) in THF (475 mL) was added at room temperature a solution of ethyl chloroformate (5.97 mL, 61.4 mmol) in THF (55 mL). After 1 h the triethylamine hydrochloride salt was filtered off and washed with a small amount of THF. The mixture was added to a solution of sodium borohydride (6.05 g, 154 mmol) and water (55 mL). After stirring overnight at room temperature aqueous sodium hydroxide solution (1 N, 180 mL) was added. Extraction with tert-butylmethylether, removal of the solvent by distillation and chromatography (silica, dichloromethane:methanol=1:0 to 95:5) afforded the title compound (11.4 g, 63%) as light yellow solid. MS: m/e=296.2 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163728B2
Source datasetuspto-grants-2012_04
ORD IDord-61c3b94bf9114632a3f3b8cd374d239a
Source noteuspto-grants-2012_04