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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2071022Generated: October 31, 2026

3-Acetyl-5-bromopyridine → 3-Bromo-5-(1-hydroxyethyl)pyridine

https://huagongshe.com/reaction/2071022

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Acetyl-5-bromopyridineHCID 820423—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
Product3-Bromo-5-(1-hydroxyethyl)pyridineHCID 1299743590.2%

Reaction Steps

To a stirred solution of 1-(5-bromopyridin-3-yl)ethanone (5.0 g, 25.0 mmol) in anhydrous MeOH (50 mL) at 0° C., was added NaBH4 (1.32 g, 35.0 mmol) and the reaction was allowed to warm to room temperature. All solvent was removed. The residue was dissolved in cold water and extracted with EtOAc (2×70 mL). The combined organic layers was dried with Na2SO4 and concentrated under reduced pressure. The residue was purified by column chromatography (40% EtOAc in hexanes) to provide 4.555 g of 1-(5-bromopyridin-3-yl)ethanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299267B2
Source datasetuspto-grants-2012_10
ORD IDord-583ae12e50e643cbbb0c01bc2fb9b1e6
Source noteuspto-grants-2012_10