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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 709776Generated: October 29, 2026

Water → (5-(Benzyloxy)-6-chloropyridin-3-yl)methanol

https://huagongshe.com/reaction/709776

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
ReactantMethyl 5-(benzyloxy)-6-chloronicotinateHCID 71496987—
SolventEthanolHCID 702—
Product(5-(Benzyloxy)-6-chloropyridin-3-yl)methanolHCID 11776027065.2%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a suspension of methyl 5-(benzyloxy)-6-chloronicotinate (3.00 g) in ethanol (40 mL) was added sodium tetrahydroborate (1.02 g), and the mixture was stirred at 60° C. for 3 hr. Water was added to the reaction mixture at 0° C., and the mixture was extracted with ethyl acetate. The extract was washed with water and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (1.76 g) as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181186B2
Source datasetuspto-grants-2015_11
ORD IDord-36cf3a47caf842aab0b359dfa59a27e2
Source noteuspto-grants-2015_11