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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1514726Generated: November 2, 2026

Triethylamine → [3-pyridin-2-yl-5([E]-styryl)-isoxazol-4-yl]-methanol

https://huagongshe.com/reaction/1514726

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
ReactantSodium HydroxideHCID 14798—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 66718302HCID 66718302—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product[3-pyridin-2-yl-5([E]-styryl)-isoxazol-4-yl]-methanolHCID 6671816972%

Reaction Steps

To a solution of 3-pyridin-2-yl-5-([E]-styryl)-isoxazole-4-carboxylic acid (1.1 g, 4 mmol) and triethylamine (0.53 mL, 4 mmol) in THF (15 mL) was added dropwise at room temperature a solution of ethyl chloroformate (0.36 mL, 4 mmol) in THF (15 mL). After 1 h the triethylamine hydrochloride salt was filtered off and washed with a small amount of THF. The filtrate was added to a solution of sodium borohydride (0.36 g, 10 mmol) in water (10 mL). After stirring for 1 h at 5° C. aqueous sodium hydroxide (2 M, 22 mL) was added. Extraction with ethyl acetate, drying over sodium sulfate, filtering and evaporation of the solvent followed by trituration with diisopropylether afforded the title compound (0.76 g, 72%) as a white solid. MS: m/e=279.2 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08222246B2
Source datasetuspto-grants-2012_07
ORD IDord-c0a5e617e74b44bea73a1da3440c846e
Source noteuspto-grants-2012_07