Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 10210Generated: October 23, 2026

Butyl vinyl ether → 1-(4-Fluoro-2-methylphenyl)ethan-1-one

https://huagongshe.com/en/reaction/10210

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyl vinyl etherHCID 8108—
ReactantPotassium CarbonateHCID 11430—
Reactant1,3-Bis(diphenylphosphino)propaneHCID 81219—
Reactant2-Bromo-5-fluorotolueneHCID 96743—
Catalystpalladium(II) acetateHCID 167845—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product1-(4-Fluoro-2-methylphenyl)ethan-1-oneHCID 349477249%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 2-bromo-5-fluorotoluene (5 g, 26.5 mmol) in DMF (65 ml) and water (15 ml) was added butyl vinyl ether (6.6 g, 65.9 mmol), palladium acetate (0.18 g, 0.8 mmol), 1,3-bis(diphenylphosphino)propane (0.72 g, 1.75 mmol) and potassium carbonate (4.4 g, 31.8 mmol). The reaction was heated at 80° C. for 48 h under nitrogen. The cooled reaction mixture was diluted with EtOAc (˜250 ml) and concentrated HCl added and shaken. Further EtOAc and water were added to obtain an easier separation of the 2 layers. The organic layer was washed with brine, dried (MgSO4), and concentrated. The residue was purified on a plug of silica eluting with 3% EtOAc/isohexane to give the title compound as an oil (1.95 g, 49%). 1H NMR (400 MHz, d6-DMSO) δ 2.45 (3H, s), 2.54 (3H, s), 7.13–7.17 (2H, m), 7.89–7.93 (1H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07094777B2
Source datasetuspto-grants-2006_08
ORD IDord-c1acfb3adf39446d8b5e3103b040d2f4
Source noteuspto-grants-2006_08