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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 922755Generated: November 1, 2026

N-bromobutanimide → 7-(Bromomethyl)-4-chloroquinoline-2-carbonitrile

https://huagongshe.com/reaction/922755

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant4-Chloro-7-methylquinoline-2-carbonitrileHCID 59774919—
CatalystBenzoyl PeroxideHCID 7187—
SolventAcetonitrileHCID 6342—
Product7-(Bromomethyl)-4-chloroquinoline-2-carbonitrileHCID 6678952457.6%

Reaction Steps

4-Chloro-7-methyl-2-quinolinecarbonitrile (1-5, 57 g, 0.37 mol, 1.0 equiv.), NBS (75 g, 0.42 mol, 1.14 equiv.) and benzoyl peroxide (0.8 g, 3.3 mmol, 0.01 equiv.) were stirred in CH3CN (30 ml, 12.3 M) at room temperature. After 16 h, the solvent was removed and the residue was partitioned between AcOEt and water, the organic layer was washed with water, dried over MgSO4 and filtered. After removal of the solvent, the residue was recrystallized from methanol to give 60 g of desired 7-(bromomethyl)-4-chloroquinoline-2-carbonitrile (2-4). LRMS m/z (M+H)+ 283.1 found, 282.9 required.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09278960B2
Source datasetuspto-grants-2016_03
ORD IDord-8372bf4412b942e7af1e3ec5bd4c880d
Source noteuspto-grants-2016_03