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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 645306Generated: October 30, 2026

1-Bromohexane → 2,6-Dibromo-1,5-bis(hexyloxy)naphthalene

https://huagongshe.com/reaction/645306

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BromohexaneHCID 8101—
Reactant1,5-Naphthalenediol, 2,6-dibromo-HCID 96260—
ReactantSodium ethoxideHCID 2723922—
SolventEthanolHCID 702—
Product2,6-Dibromo-1,5-bis(hexyloxy)naphthaleneHCID 1833210348%

Reaction Steps

Under an inert atmosphere, sodium ethoxide (2.76 g, 40.6 mmol) and 2,6-dibromo-1,5-di hydroxynaphthalene (5 g, 15.7 mmol) were dissolved in ethanol (60 ml). Under reflux, ethanol solution (10 ml) of hexylbromide (6.7 g, 40.6 mmol) was added dropwise in 10 minutes. It was refluxed for 5 hours and then left for cooling. The reaction mixture was added to 1N sodium-hydroxide aqueous solution, and the depositing precipitate was filtrated. The precipitate was washed with methylene chloride, and the washed solution was concentrated under a reduced pressure to obtain a crude product. The desired product was obtained after purifying by silica gel chromatography (toluene:hexane=4:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07701129B2
Source datasetuspto-grants-2010_04
ORD IDord-1fec327efe3a452790a109fd95f209c2
Source noteuspto-grants-2010_04