Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2401190Generated: October 30, 2026

Sodium borohydride → 1-(6-Chloropyrimidin-4-yl)ethanol

https://huagongshe.com/reaction/2401190

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant1-(6-Chloropyrimidin-4-yl)ethan-1-oneHCID 72214247—
SolventEthanolHCID 702—
Product1-(6-Chloropyrimidin-4-yl)ethanolHCID 8385410179.7%

Reaction Steps

1-(6-Chloro-4-pyrimidinyl)ethanone (Intermediate 18A, 1.0 g, 6.39 mmol) was dissolved in ethanol (21 mL), treated with sodium borohydride (0.242 g, 6.39 mmol) and the resulting mixture was stirred at room temperature under argon for 2 hours. The solvent was removed under reduced pressure and the residue was diluted with water and extracted with ethyl acetate (×3). The ethyl acetate layers were combined, dried under magnesium sulfate and evaporated under reduced pressure to give the title compound as a yellow oil (808 mg);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08796283B2
Source datasetuspto-grants-2014_08
ORD IDord-e2acdec75d9640a7ac4fac48b35ea0e7
Source noteuspto-grants-2014_08