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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1437213Generated: November 2, 2026

Diethyl Ether → 2-Fluoro-1-phenylethan-1-one

https://huagongshe.com/reaction/1437213

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantPhenacyl bromideHCID 6259—
Reactant18-Crown-6HCID 28557—
ReactantPotassium FluorideHCID 522689—
SolventAcetonitrileHCID 6342—
Product2-Fluoro-1-phenylethan-1-oneHCID 9947—

Reaction Conditions

Temperature55 °C

Reaction Steps

A suspension of potassium fluoride (3.091 g) and 18-crown-6-ether (0.341 g) in acetonitrile (25 mL) was stirred at 55° C. for 1 hour. α-Bromoacetophenone (5.12 g) was added to the reaction mixture, followed by stirring for 20 hours. Subsequently, diethyl ether was added to the reaction mixture, and then the insoluble matter that was formed was removed by filtration. Water was added for partitioning the filtrate. The organic layer was sequentially washed with water and saturated brine. Subsequently, the organic layer was dried over sodium sulfate anhydrate, followed by filtration. The solvent was evaporated under reduced pressure, to thereby give the residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07622471B2
Source datasetuspto-grants-2009_11
ORD IDord-ac3fdffeb2df48fda35063025a4d142e
Source noteuspto-grants-2009_11