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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1648183Generated: October 31, 2026

4'-Hydroxyacetophenone → 4-Ethenylphenyl acetate

https://huagongshe.com/reaction/1648183

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4'-HydroxyacetophenoneHCID 7469—
Reactant4-(1-Hydroxyethyl)phenyl acetateHCID 92345—
ReactantPotassium bisulfateHCID 516920—
Product4-Ethenylphenyl acetateHCID 75821—

Reaction Steps

p-Hydroxyacetophenone was converted to 1-(p-acetoxyphenyl)ethanol and then dehydrated using liquid phase dehydration in the presence of potassium acid sulfate to produce p-acetoxystyrene, according to the method of Corson et al (J. Org. Chem., 1958 23, 544). p-Acetoxystyrene (1.6 g) was added to a stirred solution of potassium hydroxide (1.4 g) in water (14 ml) at 5 degrees Centigrade. Stirring was continued at 0-5 degrees Centigrade for 2 h. The mixture was then washed with ether, and the aqueous phase neutralised with saturated sodium hydrogen carbonate solution. The product was extracted into dichloromethane, the solution was dried over anhydrous calcium chloride and the solvent removed, to yield a cloudy oil (0.7 g) which solidified on standing to a waxy solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05436170
Source datasetuspto-grants-1995_07
ORD IDord-eb96d01aa22340359c6782ed7b4687af
Source noteuspto-grants-1995_07