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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2067070Generated: November 2, 2026

Sodium borohydride → 1-(2-Aminopyridin-4-yl)ethanol

https://huagongshe.com/reaction/2067070

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant1-(2-Aminopyridin-4-yl)ethan-1-oneHCID 13145258—
SolventMethanolHCID 887—
Product1-(2-Aminopyridin-4-yl)ethanolHCID 1799914845.2%

Reaction Steps

To a mixture of 1-(2-aminopyridin-4-yl)ethanone (21) (168 mg, 1.234 mmol) in MeOH (10 mL), under nitrogen at 0° C., was added sodium borohydride (46.7 mg, 1.234 mmol). The resulting reaction mixture was stirred at RT for 2 hr, and then the solvents were removed under reduced pressure. The residue was taken up into EtOAc (25 mL), and extracted with saturated aq NaHCO3 solution (30 mL) and the layers separated. The aqueous layer was extracted with EtOAc (20 mL×2), and the combined organic extracts were washed with brine (30 mL), dried and the solvents removed under reduced pressure, to give 1-(2-aminopyridin-4-yl)ethanol (22) (77 mg, 45%) as a yellow oil: m/z 139 (M+H)+ (ES+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08293748B2
Source datasetuspto-grants-2012_10
ORD IDord-85bea427b38c47cfae92a61c53aae763
Source noteuspto-grants-2012_10