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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2274755Generated: October 31, 2026

Azobisisobutyronitrile → HCID 23001499, compound

https://huagongshe.com/reaction/2274755

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
Reactant2-Methoxy-4-methylquinolineHCID 84796—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 23001499HCID 23001499—

Reaction Conditions

Temperature90 °C

Reaction Steps

0.95 g (5.48 mmol) of 2-methoxy-4-methyl quinoline was dissolved in 10 mL of 1,2-dichloroethane, and then 1.17 g (6.58 mmol) of N-bromosuccinimide and 44 mg (0.27 mmol) of 2,2′-azobisisobutyronitrile were added, and stirred for 2 hours while heated at 90° C. After stirring was completed, the solution was cooled to a normal temperature, and the solvent was removed under reduced pressure to obtain 4-(bromomethyl)-2-methoxyquinoline. The obtained 4-(bromomethyl)-2-methoxyquinoline was used in a next step without any particular isolation and purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09126995B2
Source datasetuspto-grants-2015_09
ORD IDord-7a65977aac6d44dc9878399da6c06038
Source noteuspto-grants-2015_09