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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 263423Generated: October 25, 2026

4-Bromophenacyl bromide → HCID 19038041, compound

https://huagongshe.com/reaction/263423

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromophenacyl bromideHCID 7454—
Reactant5(6H)-Quinolinone, 7,8-dihydro-HCID 3016811—
SolventTolueneHCID 1140—
ProductHCID 19038041HCID 19038041—

Reaction Steps

5,6,7,8-Tetrahydroquinolin-5-one (20 g) was dissolved in 500 ml of toluene. To this solution was added 4-bromophenacyl bromide (37.8 g) gradually and refluxed for 18 hours. The reaction mixture was cooled to room temperature, and depositing solids were collected by filtration (33 g). These crystals were dissolved in 300 ml of N,N-dimethylformamide. To this solution was added, molecular sieves 3A (15 g) and triethylamine (13 ml), and the reaction mixture was heated at 100 ° C. for 1 hour. The reaction mixture became dark brown. The dark brown solution that obtained after removing insoluble matter by filtration was concentrated under reduced pressure. To the residue was added 300 ml of water and extracted with 200 ml of methylene chloride three times. The methylene chloride solution was washed with 100 ml of brine and dried over anhydrous sodium sulfate. The dark brown solution that obtained after removing drying agent by filtration was concentrated under reduced pressure, the resultant dark brown residue was purified by alumina column chromatography. The title compound was obtained as dark brown crystals (12 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05643920
Source datasetuspto-grants-1997_07
ORD IDord-37e02fa9d13b4281957b8935e8156d78
Source noteuspto-grants-1997_07