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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1514705Generated: November 2, 2026

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

https://huagongshe.com/reaction/1514705

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
ReactantSodium HydroxideHCID 14798—
ReactantSodium borohydrideHCID 4311764—
Reactant3-(3,4-Difluoro-phenyl)-5-([E]-styryl)-isoxazole-4-carboxylic acidHCID 66718191—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product[3-(3,4-Difluoro-phenyl)-5-([E]-styryl)-isoxazol-4-yl]-methanolHCID 6671818973.1%

Reaction Steps

To a solution of 3-(3,4-difluoro-phenyl)-5-([E]-styryl)-isoxazole-4-carboxylic acid (18 g, 55.0 mmol) and triethylamine (7.7 mL, 55.0 mmol) in THF (450 mL) was added at room temperature a solution of ethyl chloroformate (5.35 mL, 55.0 mmol) in THF (52 mL). After 1 h triethylamine hydrochloride salt was filtered off and washed with a small amount of THF. The solution was added to a solution of sodium borohydride (5.42 g, 138 mmol) in water (52 mL). The mixture was stirred overnight at room temperature. Sodium hydroxide solution (1 N, 180 mL) was added. Extraction with tert-butylmethylether and chromatography (silica, dichloromethane) afforded the title compound (12.6 g, 73%) as a light green solid. MS: m/e=314.2 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08222246B2
Source datasetuspto-grants-2012_07
ORD IDord-6e3ac281b24a4500aa2c2c08801d68de
Source noteuspto-grants-2012_07