HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1957533Generated: November 2, 2026
Allyl bromide → 6-(allyloxy)-3,4-dihydroquinolin-2(1H)-one
https://huagongshe.com/reaction/1957533
Participants
| Role | Name | HCID | Charge |
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| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | 6-Hydroxy-3,4-dihydro-2(1H)-quinolinone | HCID 2774040 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Potassium Hydroxide | HCID 14797 | — |
| Product | 6-(allyloxy)-3,4-dihydroquinolin-2(1H)-one | HCID 19068032 | 68.9% |
Reaction Steps
32.6 Grams of 3,4-dihydro-6-hydroxy-2(1H)-quinolinone was dissolved in 500 ml of methanol containing 12.6 g of potassium hydroxide. Under stirring this solution, 20 ml of allyl bromide was added thereto at room temperature. The reaction mixture was stirred at room temperature for 1 hour, and further stirred at 60° C. for 4 hours. After the reaction, the reaction mixture was concentrated to a half volume under reduced pressure, then 500 ml of water was added and stirred vigorously, the crystals precipitated were collected by filtration. The crystals were washed with water and small amount of diethyl ether in this order, and dried. Recrystallized from ethanol, 28 g (68.9%) of 6-allyloxy-3,4-dihydro-2(1H)-quinolinone was obtained. Colorless needle-like crystals (recrystallized from ethanol)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05786367 |
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| Source dataset | uspto-grants-1998_07 |
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| ORD ID | ord-029a50753efa4c9d9d49860005c7347b |
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| Source note | uspto-grants-1998_07 |
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