HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 495179Generated: October 25, 2026
Acetone → Methyl 3,5-diallyloxyphenylacetate
https://huagongshe.com/reaction/495179
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl 3,5-dihydroxyphenylacetate | HCID 579787 | — |
| Product | Methyl 3,5-diallyloxyphenylacetate | HCID 23116191 | 93% |
Reaction Steps
Methyl 3,5-dihydroxyphenylacetate (30 g, 0.17 mol) was dissolved in acetone (0.50 L), and potassium carbonate (91 g, 0.66 mol) and allyl bromide (0.11 L, 1.3 mol) were added thereto at room temperature. The mixture was stirred for 8 hours under heating and reflux, and then stirred at room temperature for 10 hours. The reaction mixture was concentrated under reduced pressure, and water was added to the resulting residue, followed by extraction with ethyl acetate. The organic layer was washed with a saturated aqueous solution of sodium chloride, dried over anhydrous sodium sulfate, and then concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (ethyl acetate/hexane=1/15-1/3) to obtain methyl 3,5-diallyloxyphenylacetate (40 g, 93%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07538224B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-bd46038b86e640a8860d7a95ed14d882 |
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| Source note | uspto-grants-2009_05 |
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