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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 503140Generated: October 29, 2026

4-Fluorophenol → 1-(2,2-Diethoxyethoxy)-4-fluorobenzene

https://huagongshe.com/reaction/503140

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-FluorophenolHCID 9732—
ReactantPotassium CarbonateHCID 11430—
ReactantEthane, 2-bromo-1,1-diethoxy-HCID 74852—
SolventAcetoneHCID 180—
Product1-(2,2-Diethoxyethoxy)-4-fluorobenzeneHCID 11447518—

Reaction Conditions

Temperature120 °C

Reaction Steps

To a solution of 10.0 g of 4-fluorophenol and 16.1 ml of bromoacetaldehyde diethylacetal in 100 ml dimethylformaldehyde was added 18.5 g of potassium carbonate at room temperature, and the mixture was stirred at 120° C. for two days. The reaction mixture was filtered through Celite, and the filtrate was diluted with ethyl acetate. The organic layer was sequentially washed with saturated aqueous ammonium chloride solution and brine, dried over anhydrous magnesium sulfate and the solvent was evaporated. The crude product was purified and separated by silica gel column chromatography (ethyl acetate:n-hexane=0:10 to 1:20), to give 17.3 g of the title compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07776890B2
Source datasetuspto-grants-2010_08
ORD IDord-9b798ee227b84dec8d4c1654f51162f5
Source noteuspto-grants-2010_08