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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 963953Generated: October 30, 2026

4-(1-Hydroxyethyl)phenyl acetate → 4-Ethenylphenyl acetate

https://huagongshe.com/reaction/963953

Reaction equation

Participants

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

Reaction Steps

p-Hydroxyxstyrene 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 anydrous 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 numberUS05766960
Source datasetuspto-grants-1998_06
ORD IDord-7bbf977ee29747c4848b6643beeb6d56
Source noteuspto-grants-1998_06