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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1916808Generated: October 26, 2026

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

https://huagongshe.com/reaction/1916808

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 numberUS08618140B2
Source datasetuspto-grants-2013_12
ORD IDord-b8d9497fde23420f91443ef216f526a3
Source noteuspto-grants-2013_12