HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1938136Generated: October 28, 2026
4'-Hydroxyacetophenone → 4-Ethenylphenyl acetate
https://huagongshe.com/reaction/1938136
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4'-Hydroxyacetophenone | HCID 7469 | — |
| Reactant | 4-(1-Hydroxyethyl)phenyl acetate | HCID 92345 | — |
| Reactant | Potassium bisulfate | HCID 516920 | — |
| Product | 4-Ethenylphenyl acetate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05693477 |
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| Source dataset | uspto-grants-1997_12 |
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| ORD ID | ord-b5845c969a6c412ab41855ca2081b690 |
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| Source note | uspto-grants-1997_12 |
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