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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2422525Generated: November 3, 2026

Azobisisobutyronitrile → 7-(Bromomethyl)-4-phenylquinoline-2-carbonitrile

https://huagongshe.com/reaction/2422525

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
Reactant7-Methyl-4-phenylquinoline-2-carbonitrileHCID 57437831—
SolventCarbon TetrachlorideHCID 5943—
Product7-(Bromomethyl)-4-phenylquinoline-2-carbonitrileHCID 57437832—

Reaction Steps

A solution of 7-methyl-4-phenylquinoline-2-carbonitrile (11.2 g, 41.7 mmol), N-bromo-succinimide (12.2 g, 68.6 mmol) and AIBN (2,2′-azobisisobutyronitrile) (200 mg) in carbon tetrachloride (200 mL) was heated at reflux overnight. The reaction was cooled to ambient temperature and the solid residue was filtered. The filtrate was concentrated under reduced pressure. The crude product was purified by flash column chromatography (eluting with 5% ethyl acetate in hexane) to give the title compound. 1H NMR (400 MHz, acetone-d6): δ 8.30 (s, 1H), 8.06 (d, 1H), 7.90 (s, 1H), 7.87 (d, 1H), 7.6-7.7 (m, 5H), 4.95 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960409B2
Source datasetuspto-grants-2011_06
ORD IDord-ad51e95d5f2a4fe887226f09a875a790
Source noteuspto-grants-2011_06