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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 872409Generated: October 26, 2026

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

https://huagongshe.com/reaction/872409

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 numberUS08975285B2
Source datasetuspto-grants-2015_03
ORD IDord-b0ee208866054cd0bebe63a8c6e36b21
Source noteuspto-grants-2015_03