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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 413474Generated: October 28, 2026

Sodium borohydride → (2-Chloro-5-methylpyridin-3-yl)methanol

https://huagongshe.com/reaction/413474

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant2-Chloro-5-methylpyridine-3-carbaldehydeHCID 9834018—
SolventMethanolHCID 887—
Product(2-Chloro-5-methylpyridin-3-yl)methanolHCID 1205672188%

Reaction Steps

Sodium borohydride (0.65 g, 0.0167 moles) was added slowly to a well-stirred solution of 2-chloro-5-methylpyridine-3-carbaldehyde (1.3 g, 0.0084 moles) in methanol (20 ml) at 0° C. temperature over a period of 15 minutes. The reaction mass was further stirred for 2 hours at the same temperature. The solvent was removed under reduced pressure and the mass was quenched with water (25 ml). The mass was extracted with ethyl acetate (2×50 ml) and the layers separated. The organic layer was removed under reduced pressure. The residue so obtained was subjected to chromatographic purification on silica gel to give 2-chloro-3-hydroxymethyl-5-methylpyridine as a solid in 88 % yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06566528B1
Source datasetuspto-grants-2003_05
ORD IDord-55e33fcc56a84aee8883be0977b9913f
Source noteuspto-grants-2003_05