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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2058200Generated: November 1, 2026

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

https://huagongshe.com/reaction/2058200

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 numberUS04215126
Source datasetuspto-grants-1980_07
ORD IDord-b791215d02b5430e9ba8c0f68196d8e5
Source noteuspto-grants-1980_07