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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1695440Generated: October 30, 2026

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

https://huagongshe.com/reaction/1695440

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
ReactantSodium HydroxideHCID 14798—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 66643754HCID 66643754—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product[3-(4-Chloro-phenyl)-5-([E]-styryl)-isoxazol-4-yl]-methanolHCID 6664381479%

Reaction Steps

To a solution of 3-(4-chloro-phenyl)-5-([E]-styryl)-isoxazole-4-carboxylic acid (6.0 g, 18.4 mmol) and triethylamine (2.58 mL, 18.4 mmol) in THF (150 mL) was added at room temperature a solution of ethyl chloroformate (1.8 mL, 18.4 mmol) in THF (17.4 mL). After 1 h triethylamine hydrochloride salt was filtered off, and washed with a small amount of THF. The solution was then added to a solution of sodium borohydride (1.82 g, 46.1 mmol) in water (18 mL). After stirring overnight at room temperature sodium hydroxide solution (1 N) was added. Extraction with tert-butylmethylether and purification by chromatography (silica, dichloromethane) afforded the title compound (4.52 g, 79%) as a white solid. MS: m/e=369.9 [M+CH3COO]−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163728B2
Source datasetuspto-grants-2012_04
ORD IDord-52d14c1eed5c4efe839fe9a82ad314b3
Source noteuspto-grants-2012_04