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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1636177Generated: October 26, 2026

2-(Benzyloxy) ethanol → 2-(2-(Benzyloxy)ethoxy)-6-bromopyridine

https://huagongshe.com/reaction/1636177

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Benzyloxy) ethanolHCID 12141—
Reactant2,6-DibromopyridineHCID 12274—
ReactantSodium hydrideHCID 24758—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product2-(2-(Benzyloxy)ethoxy)-6-bromopyridineHCID 18673828—

Reaction Steps

Sodium hydride (900 mg, 60% dispersion in mineral oil, 22.5 mmol) was added portionwise to an ice-cold solution of 2-(benzyloxy)ethanol (3.0 g, 20.0 mmol) in toluene (100 ml), and the solution stirred for 30 minutes. 2,6-Dibromopyridine (4.75 g, 20.0 mmol) was added, and the reaction heated under reflux for 2 hours. The cooled mixture was diluted with water (100 ml), and extracted with ethyl acetate (3×100 ml). The combined organic extracts were dried (MgSO4), filtered and evaporated in vacuo to give the title compound as a yellow oil, (quantitative).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06511993B1
Source datasetuspto-grants-2003_01
ORD IDord-660881e9aa194da2a4c87925444ad01e
Source noteuspto-grants-2003_01