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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 17933Erstellt: 24. Oktober 2026

6-Methylquinoline → 6-(Bromomethyl)quinoline

https://huagongshe.com/de/reaction/17933

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt6-MethylquinolineHCID 7059—
EduktBenzoyl PeroxideHCID 7187—
EduktN-bromobutanimideHCID 67184—
LösungsmittelCarbon TetrachlorideHCID 5943—
Produkt6-(Bromomethyl)quinolineHCID 22439654%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07741321B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-bdab12189dab47a7a6bf709c59d3a49b
Quellennotizuspto-grants-2010_06