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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 707641Generated: October 28, 2026

Sodium borohydride → 3-(2-Pyridinyl)-5-isoxazolemethanol

https://huagongshe.com/reaction/707641

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantEthyl 3-(pyridin-2-yl)isoxazole-5-carboxylateHCID 58062833—
SolventEthanolHCID 702—
Product3-(2-Pyridinyl)-5-isoxazolemethanolHCID 686542—

Reaction Conditions

Temperature30 °C

Reaction Steps

To a mixture of 2-(5-ethoxycarbonyl-isoxazol-3-yl)-pyridine (6.5 gm), in ethanol (80 ml) was added sodium borohydride (2 gm) in lots at 30° C. It was stirred at 30° C. over a period of 1.5 h. The reaction was monitored by TLC. Upon consumption of starting material, aqueous ammonium chloride solution was added. The mixture was extracted with ethyl acetate. Combined organic layers was washed with water and concentrated under vacuum to provide title compound in 7.7 gm quantity. It was purified by using silica gel column chromatography to afford tile compound in 4.5 g (85%) quantity as off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09175031B2
Source datasetuspto-grants-2015_11
ORD IDord-a1ca6f835c69490096330e81b8413deb
Source noteuspto-grants-2015_11