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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2035793Generated: October 31, 2026

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

https://huagongshe.com/reaction/2035793

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 numberUS08575154B2
Source datasetuspto-grants-2013_11
ORD IDord-c0786f9f3eea4cdb82bb1a0ff30350d7
Source noteuspto-grants-2013_11