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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 401542Erstellt: 25. Oktober 2026

6-Methylquinoline → 6-(Bromomethyl)quinoline

https://huagongshe.com/reaction/401542

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
PatentnummerUS08741933B2
Quelldatensatzuspto-grants-2014_06
ORD IDord-dfc90552ad7e46b4ba96c3c1888ce720
Quellennotizuspto-grants-2014_06