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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1505105Generated: November 3, 2026

6-Methylquinoline → 6-(Bromomethyl)quinoline

https://huagongshe.com/reaction/1505105

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 numberUS09216969B2
Source datasetuspto-grants-2015_12
ORD IDord-9bf9b76fc8c74823a4856227ad122a1d
Source noteuspto-grants-2015_12