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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 263233Generated: October 28, 2026

Methanol → (3-Methoxypyridin-2-yl)methanol

https://huagongshe.com/reaction/263233

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium borohydrideHCID 4311764—
ReactantMethyl 3-methoxypyridine-2-carboxylateHCID 20474189—
SolventEthanolHCID 702—
Product(3-Methoxypyridin-2-yl)methanolHCID 532477457.5%

Reaction Steps

Sodium borohydride (6.3 g) was added slowly over 75 minutes to a solution of 3-methoxy-2-methoxycarbonylpyridine (9.2 g) in ethanol. Methanol (100 ml) was then added and after the initial vigorous reaction had subsided, further sodium borohydride (8.3 g) was added over a further 3 hours, and the mixture was left to stand overnight. The solvent was evaporated, the residue dissolved in water and extracted with chloroform and the chloroform solution dried. Evaporation, and crystallisation from ether gave 2-hydroxymethyl-3-methoxypyridine (4.4 g) m.p. 72.5°-73.5°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04156727
Source datasetuspto-grants-1979_05
ORD IDord-d9439c4128894b84b47ff4f269566fc6
Source noteuspto-grants-1979_05