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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1684574Generated: November 1, 2026

Azobisisobutyronitrile → 3-Benzoyl-2-bromomethyl-4-(3,4-dimethoxyphenyl)-6,7-dimethoxyquinoline

https://huagongshe.com/reaction/1684574

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 19039879HCID 19039879—
SolventCarbon TetrachlorideHCID 5943—
Product3-Benzoyl-2-bromomethyl-4-(3,4-dimethoxyphenyl)-6,7-dimethoxyquinolineHCID 1903991142.1%

Reaction Steps

A mixture of 3-benzoyl-4-(3,4-dimethoxyphenyl)-6,7-dimethoxy-2-methylquinoline (5.5 g), N-bromosuccinimide (2.42 g), 2,2'-azobis(isobutyronitrile)(0.815 g) and carbon tetrachloride (250 ml) was stirred under reflux for 1.5 hours. The reaction mixture was cooled, and then the insoluble material was filtered off. The filtrate was washed with water and dried over magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was subjected to column chromatography on silica gel. The fractions eluted with chloroform-ethyl acetate (10:1, v/v) gave 3-benzoyl-2-bromomethyl-4-(3,4-dimethoxyphenyl)-6,7-dimethoxyquinoline (2.73 g, 42%). This compound was recrystallized from ethyl acetate-hexane to give colorless prisms, mp. 182°-183° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05641788
Source datasetuspto-grants-1997_06
ORD IDord-169bdaf4e5164459a3bc533f19ae0dce
Source noteuspto-grants-1997_06