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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 219050Generated: October 26, 2026

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

https://huagongshe.com/reaction/219050

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, 5eq) 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 numberUS08198483B2
Source datasetuspto-grants-2012_06
ORD IDord-c27e97d533db48f29b8bb76197b9ff57
Source noteuspto-grants-2012_06