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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1173976Generated: October 25, 2026

Azobisisobutyronitrile → 6-(Bromomethyl)-2-methylquinoline

https://huagongshe.com/reaction/1173976

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
Reactant2,6-DimethylquinolineHCID 13414—
ReactantN-bromobutanimideHCID 67184—
SolventCarbon TetrachlorideHCID 5943—
Product6-(Bromomethyl)-2-methylquinolineHCID 279548027.4%

Reaction Steps

In carbon tetrachloride (26 ml), 2,6-dimethylquinoline (manufactured by Tokyo Kasei Kogyo Co., Ltd.) (1.0398 g), N-bromosuccinimide (1.2353 g), and azobisisobutyronitrile (98.5 mg) were dissolved and then the whole was subjected to thermal reflux for 2 hours under an argon atmosphere. After the reaction, a precipitate was removed through filtration and then washed with water, followed by drying with magnesium sulfate. The solvent was distilled off and the residue was then purified through silica gel column chromatography (hexane/ethyl acetate), thereby obtaining the subject compound (427.3 mg) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07833991B2
Source datasetuspto-grants-2010_11
ORD IDord-621068ad687841ff8c58d580112f94c8
Source noteuspto-grants-2010_11