Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1038563Generated: October 31, 2026

4'-Hydroxyacetophenone → HCID 3026312, compound

https://huagongshe.com/reaction/1038563

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4'-HydroxyacetophenoneHCID 7469—
Reactant3-Chloro-2-methyl-1-propeneHCID 11241—
ReactantPotassium CarbonateHCID 11430—
CatalystTetrabutylammonium IodideHCID 67553—
SolventAcetoneHCID 180—
ProductHCID 3026312HCID 302631290%

Reaction Conditions

Temperature70 °C

Reaction Steps

1-(4-Hydroxyphenyl)ethanone (1.36 g, 10 mmol) was dissolved in acetone (50 mL), tetrabutyl ammonium iodide (370 mg, 1.0 mmol), potassium carbonate (2.76 g, 20 mmol) and 3-chloro-2-methyl-1-propene (1.5 mL, 15 mmol) were added sequentially, and the mixture was stirred at 70° C. overnight. The reaction solution was filtered, washed with acetone and concentrated in vacuo. The obtained residue was added water and ethyl acetate, and extracted with ethyl acetate. The organic layer was washed with 1N-aqueous solution of sodium hydroxide and brine, dried over anhydrous sodium sulfate, and concentrated in vacuo. 1-(4-(2-Methylallyloxy)phenyl)ethanone (1.71 g (yield 90%)) was obtained as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08551985B2
Source datasetuspto-grants-2013_10
ORD IDord-e78541b7ccdc458c877fa4e467a23986
Source noteuspto-grants-2013_10