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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1405706Generated: November 2, 2026

Ethanol → (2-Chloropyridin-3-yl)methanol

https://huagongshe.com/reaction/1405706

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantTetrahydrofuranHCID 8028—
ReactantMethyl 2-chloronicotinateHCID 819931—
ReactantSodium borohydrideHCID 4311764—
SolventWaterHCID 962—
Product(2-Chloropyridin-3-yl)methanolHCID 276364777%

Reaction Steps

To a mixture of methyl 2-chloronicotinate (5 g), dehydrated THF (30 mL) and ethanol (30 mL) was added sodium borohydride (4.41 g) at 0° C. The reaction mixture was stirred at room temperature overnight, poured into water, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (3.22 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08916551B2
Source datasetuspto-grants-2014_12
ORD IDord-43449beff2c64308bc81f88cc5003c45
Source noteuspto-grants-2014_12