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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2369667Generated: October 31, 2026

Water → [(2-[(6-Bromohexyl)oxy]ethoxy)methyl]benzene

https://huagongshe.com/reaction/2369667

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-(Benzyloxy) ethanolHCID 12141—
Reactant1,6-DibromohexaneHCID 12368—
ReactantSodium HydroxideHCID 14798—
CatalystTetrabutylammonium BromideHCID 74236—
Product[(2-[(6-Bromohexyl)oxy]ethoxy)methyl]benzeneHCID 46833105—

Reaction Steps

A solution of 2-(benzyloxy)ethanol (2.00 g) and tetrabutylammonium bromide (84 mg) in 1,6-dibromohexane (6.06 ml) was treated with 50% w/v sodium hydroxide solution (5.0 ml) and the mixture was vigorously stirred for 18 h at 20°. Water (50 ml) was added and the mixture was extracted with dichloromethane (40 ml). The organic extract was dried (Na2SO4) and the solvent evaporated in vacuo to give a residue which was purified by flash chromatography on silica gel. Elution with EtOAc-PE (1:9) gave the title compound (2.87 g). LCMS RT=3.94 min, ES+ve 337 (MNa)+, 339 (MNa)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE044874E1
Source datasetuspto-grants-2014_04
ORD IDord-cc8dc3714b504e1b95cf77c2d332ba5b
Source noteuspto-grants-2014_04