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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1031424Generated: November 2, 2026

Sodium borohydride → [6-(1H-Imidazol-1-yl)pyridin-3-yl]methanol

https://huagongshe.com/reaction/1031424

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactantmethyl 6-(1H-imidazol-1-yl)nicotinateHCID 4315458—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product[6-(1H-Imidazol-1-yl)pyridin-3-yl]methanolHCID 14207630—

Reaction Steps

NaBH4 (37.82 g) is added portionwise to a suspension of the imidazolyl ester of Step 2. above (9.98 g) in methanol at about 0.° C. The reaction mixture is heated to reflux for 71/2 hours, allowed to cool and stand 15 hours. Water (75 ml) is added, and the quenched reaction mixture evaporated, affording a solid residue which is suspended in water, extracted with chloroform dried over Na2SO4, filtered and evaporated, recrystallized (CHCl3), affording the desired product as a white solid. M.P.=128.5°-130° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04954494
Source datasetuspto-grants-1990_09
ORD IDord-7e8ddf07c3a64967b0a43b4e4f2eeb12
Source noteuspto-grants-1990_09