Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1957536Generated: November 2, 2026

4-Bromoanisole → 6-allyloxy-3,4-dihydro-1-(4-methoxyphenyl)-2(1H)-quinolinone

https://huagongshe.com/reaction/1957536

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromoanisoleHCID 7730—
ReactantSodium hydrideHCID 24758—
Reactant6-(allyloxy)-3,4-dihydroquinolin-2(1H)-oneHCID 19068032—
SolventDimethylformamideHCID 6228—
Product6-allyloxy-3,4-dihydro-1-(4-methoxyphenyl)-2(1H)-quinolinoneHCID 1906799442%

Reaction Conditions

Temperature120 °C

Reaction Steps

2 Grams of 6-allyloxy-3,4-dihydro-2(1H)-quinolinone was dissolved in 50 ml of dimethyl-formamide, then 0.5 g of 60% oily sodium hydride and 5 ml of p-bromoanisole were added thereto by the procedures similar to those employed in Reference example 7, further 4 g of cuprous chloride was added, and stirred at 120° C. for 24 hours. The inorganic materials were removed by filtration, and the filtrate was concentrated under reduced pressure. Thus obtained residual product was subjected to extraction with 200 ml of methylene chloride, the extract was washed with water and an aqueous solution saturated with sodium chloride. Then the extract was concentrated and subjected to purification by passing through a silica gel column, there was obtained 1.3 g (42%) of 6-allyloxy-3,4-dihydro-1-(4-methoxyphenyl)-2(1H)-quinolinone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05786367
Source datasetuspto-grants-1998_07
ORD IDord-109cae1271d045e58684438be1860755
Source noteuspto-grants-1998_07