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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1916627Generated: October 25, 2026

Azobisisobutyronitrile → 6-Bromo-2-(bromomethyl)quinoline

https://huagongshe.com/reaction/1916627

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
Reactant6-Bromo-2-methylquinolineHCID 522885—
SolventCarbon TetrachlorideHCID 5943—
Product6-Bromo-2-(bromomethyl)quinolineHCID 58970532—

Reaction Steps

148 mg (1.00 mmol) α,α-azoisobutyronitrile and 8.01 g (45.0 mmol) N-bromosuccinimide are added successively to a solution of 10.0 g (45.0 mmol) 6-bromo-2-methyl-quinoline in 60 mL carbon tetrachloride. The reaction mixture is refluxed for 8 h. It is filtered and the filtrate is washed twice with water. The organic phase is dried over MgSO4 and the solvent is eliminated i.vac. The purification is carried out by column chromatography on silica gel (PE/EtOAc 4:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618132B2
Source datasetuspto-grants-2013_12
ORD IDord-eeef34e06cb945688a8dc1fc86e388de
Source noteuspto-grants-2013_12