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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2041232Generated: November 2, 2026

8-Methylquinoline → 8-(Bromomethyl)quinoline

https://huagongshe.com/reaction/2041232

Reaction equation

Participants

RoleNameHCIDCharge
Reactant8-MethylquinolineHCID 11910—
ReactantN-bromobutanimideHCID 67184—
CatalystBenzoyl PeroxideHCID 7187—
SolventCarbon TetrachlorideHCID 5943—
Product8-(Bromomethyl)quinolineHCID 34691483.7%

Reaction Steps

Combine 8-methyl-quinoline (1.0 g, 6.99 mmol), NBS (1.3 g, 7.13 mmol), benzoyl peroxide (6.0 mg, 0.03 mmol), carbon tetrachloride (30 mL) and reflux for 17 h. Cool the reaction mixture to ambient temperature and evaporate the solvent. Dissolve the residue in chloroform (30 mL), wash the organic solution with saturated aqueous NaHCO3 (2×10 mL), brine (10 mL) and dry over anhydrous Na2SO4. Evaporate the solvent and purify by chromatography on silica gel eluting with DCM to obtain the title compound as a white solid (1.3 g, 83%). MS (ES+) m/z: 223 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580780B2
Source datasetuspto-grants-2013_11
ORD IDord-f914b64b5b6c44ddb836214348aa54f3
Source noteuspto-grants-2013_11