HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 26038Generated: October 25, 2026
Chloroacetone → Acetonyl 4-hydroxyphenylpropionate
https://huagongshe.com/reaction/26038
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroacetone | HCID 6571 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-(4-Hydroxyphenyl)propionic acid | HCID 102526 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | Acetonyl 4-hydroxyphenylpropionate | HCID 21326463 | 97% |
Reaction Steps
After 49.9 g of 4-hydroxyphenylpropionic acid was dissolved in 160 ml of dimethylformamide, 21.8 g of potassium carbonate was added to the solution at room temperature. Then 29.1 g of monochloroacetone was added dropwise to the solution at 60° C. and the reaction with 4-hydroxyphenylpropionic acid was carried out at 80°-90° C. for 1 hour. After the reaction, dimethylformamide was distilled off from the reaction solution to give a residue. After the residue was dissolved in dichloroethane, the solution was washed with water. The layer of dichloroethane was removed and the solvent was distilled off to give 64.7 g (yield 97%) of acetonyl 4-hydroxyphenylpropionate. After recrystallization from isopropylether, the product was a colorless crystalline material having a melting point of 64.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04147876 |
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| Source dataset | uspto-grants-1979_04 |
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| ORD ID | ord-75c5bea0e4de42d1a60057506ce3ec87 |
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| Source note | uspto-grants-1979_04 |
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