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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 503091Generated: November 2, 2026

Water → 2-((2-((6-Bromohexyl)oxy)ethoxy)methyl)-1,3-dichlorobenzene

https://huagongshe.com/reaction/503091

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1,6-DibromohexaneHCID 12368—
ReactantSodium HydroxideHCID 14798—
ReactantEthanol, 2-((2,6-dichlorophenyl)methoxy)-HCID 13341669—
CatalystTetrabutylammonium BromideHCID 74236—
SolventTolueneHCID 1140—
Product2-((2-((6-Bromohexyl)oxy)ethoxy)methyl)-1,3-dichlorobenzeneHCID 6684490361.2%

Reaction Steps

50% aq NaOH (1.89 L), 2-(2,6-dichlorobenzyloxy)ethanol (473.2 g), 1,6-dibromohexane (2.44 kg, 5 eq) and tetrabutylammonium bromide (34.1 g, 5 mol %) in toluene (1.89 L) was heated to 55-60° C. for 8-20 h. On cooling water (558 mL) and toluene (558 mL) were added. The aqueous phase was separated and diluted with water (1 L) then back extracted with toluene (1.1 L). The combined toluene extracts were washed twice with water (2.2 L), then evaporated to dryness on a rotary evaporator. The excess 1,6-dibromohexane was removed using a wiped film evaporator, and the resulting crude product chromatographed on silica (5 kg Biotage), eluting with 5% ethyl acetate in petrol 60/80, to give the title compound (503.2 g)−LC RT=7.0 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07776895B2
Source datasetuspto-grants-2010_08
ORD IDord-8876ba81f9c2443ba8afedb8d6b7da4e
Source noteuspto-grants-2010_08