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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2304825Generated: November 3, 2026

Benzyl Bromide → Hexaethylene Glycol Monobenzyl Ether

https://huagongshe.com/reaction/2304825

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantHexaethylene GlycolHCID 17472—
SolventWaterHCID 962—
SolventSodium HydroxideHCID 14798—
ProductHexaethylene Glycol Monobenzyl EtherHCID 11164646—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of hexaethylene glycol (Aldrich, 100 g) and benzyl bromide (Aldrich, 12 g) in aqueous sodium hydroxide (50% (w/w), 80 ml) was stirred at 100° C. (oil bath) under nitrogen for 2 h. The reaction mixture was then cooled to ambient temperature, diluted with water to a total volume of 500 ml, and extracted with diethyl ether (200 ml) to remove dibenzylated product. Sodium chloride (100 g) was added to the aqueous layer, which was extracted further with diethyl ether (6×100 ml). These ether extracts were combined, dried (sodium sulfate), and concentrated to give hexaethylene glycol monobenzyl ether as an oil (25 g, 20% based on glycol), 1H-NMR (CDCl3) δ: 7.30 (m, 5, 5 phenyl CH), 4.53 (s, 2, benzyl CH2), 3.69-3.54 (m, 22, 11 OCH2), 3.06 (br s, 3, OH and CH2O).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06437124B1
Source datasetuspto-grants-2002_08
ORD IDord-10670cd6a3834b93a9aeb11eb5794afe
Source noteuspto-grants-2002_08