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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2069043Generated: October 30, 2026

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

https://huagongshe.com/reaction/2069043

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 (36) (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 reaction mixture was stirred at RT for 2 hr, and the volatiles were removed under reduced pressure. The residue was taken up into EtOAc (25 mL), and extracted with saturated aq NaHCO3 solution (30 mL). The aqueous layer was back extracted with EtOAc (2×20 mL), and the combined organic extracts were washed with brine (30 mL), dried and the solvents removed in vacuo to give the title compound (37) (77 mg, 45%) as a yellow oil: m/z 139 (M+H)+ (ES+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299073B2
Source datasetuspto-grants-2012_10
ORD IDord-e8ffde79d0ec4b459c7a4f1d51564ab6
Source noteuspto-grants-2012_10