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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1255281Generated: October 31, 2026

Ethylene Glycol → 2-(3-Bromobenzyloxy)ethanol

https://huagongshe.com/reaction/1255281

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
ReactantSodium hydrideHCID 24758—
Reactant3-Bromobenzyl bromideHCID 69979—
CatalystTetrabutylammonium IodideHCID 67553—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2-(3-Bromobenzyloxy)ethanolHCID 57956818—

Reaction Steps

Sodium hydride (60% suspension in mineral oil, 1.23 g) was added portionwise to a solution of ethane-1,2-diol (4.7 mL) in THF (70 mL) and the mixture was stirred at RT for 30 min. 1-Bromo-3-(bromomethyl)benzene (7 g) was added, followed by tetrabutylammonium iodide (1.03 g) and the reaction mixture was heated at reflux for 90 min. The mixture was diluted with water and extracted into ethyl acetate (×2). The combined organics were dried over MgSO4, filtered and evaporated. The crude product was purified by silica chromatography using 30% ethyl acetate in isohexane as solvent to afford the subtitled compound as a colourless oil. Yield 4.90 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08455483B2
Source datasetuspto-grants-2013_06
ORD IDord-5692a6dab6d34d51857d23def6684ccb
Source noteuspto-grants-2013_06