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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384450Generated: October 31, 2026

Water → 1-[4-(Benzyloxy)butoxy]-4-fluorobenzene

https://huagongshe.com/reaction/384450

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-FluorophenolHCID 9732—
ReactantPotassium CarbonateHCID 11430—
Reactant((4-Bromobutoxy)methyl)benzeneHCID 4422181—
SolventDimethylformamideHCID 6228—
Product1-[4-(Benzyloxy)butoxy]-4-fluorobenzeneHCID 5952751669.6%

Reaction Conditions

Temperature100 °C

Reaction Steps

4-Fluorophenol (500 mg) and benzyl 4-bromobutyl ether (1.1 g) were dissolved in DMF (20 mL), and potassium carbonate (1.0 g) was added thereto at room temperature, followed by stirring at 100° C. for 18 hours. The reaction mixture was allowed to cool to room temperature, and water was added thereto, followed by extraction with ethyl acetate. The organic layer was washed sequentially with water and saturated brine and dried over anhydrous sodium sulfate, and the solvent was evaporated. The residue was purified by silica gel column chromatography (eluent: hexane/ethyl acetate=90/10) to obtain 1-[4-(benzyloxy)butoxy]-4-fluorobenzene (851 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367702B2
Source datasetuspto-grants-2013_02
ORD IDord-52a0c517beb1424fa6d9f0db3c9eb3c7
Source noteuspto-grants-2013_02