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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1008812Generated: November 2, 2026

6-Methylquinoline → 6-(Bromomethyl)quinoline

https://huagongshe.com/reaction/1008812

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 numberUS07973038B2
Source datasetuspto-grants-2011_07
ORD IDord-fd0684e212c44740b31514534aa9a42c
Source noteuspto-grants-2011_07