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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Ethyl 3-(pyridin-2-yl)isoxazole-5-carboxylate | HCID 58062833 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-(2-Pyridinyl)-5-isoxazolemethanol | HCID 686542 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09175031B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-a1ca6f835c69490096330e81b8413deb |
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| Source note | uspto-grants-2015_11 |
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