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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2188853Generated: November 1, 2026

6-Methylquinoline → 6-(Bromomethyl)quinoline

https://huagongshe.com/reaction/2188853

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-MethylquinolineHCID 7059—
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
SolventCarbon TetrachlorideHCID 5943—
Product6-(Bromomethyl)quinolineHCID 22439654%

Reaction Steps

To a solution of 6-methylquinoline (2.15 g, 15.0 mmol) in CCl4 (30 mL) was added NBS (2.92 g, 16.5 mmol) and benzoyl peroxide (BP, 0.36 g, 1.5 mmol) at room temperature. The mixture was heated at reflux for 2 hours. After cooling, the mixture was evaporated under vacuum to give a yellow solid, which was extracted with Petroleum Ether (30 mL×5). The extracts were concentrated under vacuum to give crude 6-bromomethylquinoline (1.8 g), which was used directly in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324207B2
Source datasetuspto-grants-2012_12
ORD IDord-da37a3ba7b414ee49a71cc046b3bba4a
Source noteuspto-grants-2012_12