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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
Reactant6-Hydroxy-3,4-dihydro-2(1H)-quinolinoneHCID 2774040—
SolventMethanolHCID 887—
SolventPotassium HydroxideHCID 14797—
Product6-(allyloxy)-3,4-dihydroquinolin-2(1H)-oneHCID 1906803268.9%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05786367
Source datasetuspto-grants-1998_07
ORD IDord-029a50753efa4c9d9d49860005c7347b
Source noteuspto-grants-1998_07