HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1611897Generated: October 26, 2026
Ethyl benzoylacetate → 4-Penten-1-one, 1-phenyl-
https://huagongshe.com/reaction/1611897
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl benzoylacetate | HCID 7170 | — |
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Penten-1-one, 1-phenyl- | HCID 101362 | 98% |
| Product | Sodium | HCID 5360545 | — |
Reaction Steps
A sodium solution of alcohol was prepared by dissolving 33 g of sodium in 1000 mL of ethanol. To the warm solution, 260 mL of benzoyl-acetic acid-ethylester was added and then 130 mL of allyl bromide was slowly dropped into the solution. The mixture was refluxed for 4 hrs. and then the solid removed in a vacuum. The resulting solid was then combined in an aqueous solution of potassium hydroxide prepared by combining 145 g of potassium hydroxide with 500 mL of water. This mixture was heated under reflux for 4 hrs. The mixture was then neutralized and extracted three times with 150 mL of diethylether. The organic layer was separated, washed twice with water, and dried. The solvent was removed in a vacuum to produce a 98 percent yield of phenyl-(but-3-enyl) ketone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06992035B2 |
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| Source dataset | uspto-grants-2006_01 |
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| ORD ID | ord-b497c97bcb2341b6b6c9000bad0bb20b |
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| Source note | uspto-grants-2006_01 |
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