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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1514672Generated: November 4, 2026

Sodium borohydride → HCID 66718147, compound

https://huagongshe.com/reaction/1514672

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 86646253HCID 86646253—
SolventMethanolHCID 887—
ProductHCID 66718147HCID 6671814789%

Reaction Steps

A solution of 6-(5-formyl-3-phenyl-isoxazol-4-ylmethoxy)-nicotinic acid methyl ester (0.25 g, 0.74 mmol) in methanol (10 mL) was treated at room temperature with sodium borohydride (0.03 g, 0.74 mmol) and stirred for 1 h. After quenching with aqueous citric acid (5 mL of a 10% solution) and extraction with ethyl acetate the organic phase was dried (Na2SO4) filtered and concentrated. Purification by chromatography (silica, heptane:ethyl acetete=90:10 to 40:60) afforded the title compound as a white solid (0.22 g, 89%). MS: m/e=341.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08222246B2
Source datasetuspto-grants-2012_07
ORD IDord-b521316f22974416a5f3885d5f17d784
Source noteuspto-grants-2012_07