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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 17933Generated: October 26, 2026

6-Methylquinoline → 6-(Bromomethyl)quinoline

https://huagongshe.com/reaction/17933

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 numberUS07741321B2
Source datasetuspto-grants-2010_06
ORD IDord-bdab12189dab47a7a6bf709c59d3a49b
Source noteuspto-grants-2010_06