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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 7135Erstellt: 24. Oktober 2026

3-Bromoquinoline → 3-Methoxyquinoline

https://huagongshe.com/de/reaction/7135

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-BromoquinolineHCID 21413—
EduktSodium MethoxideHCID 10942334—
LösungsmittelDimethylformamideHCID 6228—
Produkt3-MethoxyquinolineHCID 5758076,2%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

A solution of 3-bromoquinoline (22.54 g, 108 mmol) in anhydrous DMF (110 mL) was treated with sodium methoxide (11.70 g, 217 mmol) and stirred at 80° C. for 16 hours. The reaction mixture was then concentrated and the residue taken up in ethyl acetate (300 mL) and water (60 mL). The organic phase was separated, washed with brine (2×60 mL), dried (MgSO4), filtered, concentrated and purified by column chromatography on silica gel (ethyl acetate/hexane; 1:3) to give 3-methoxyquinoline (1.06 g, 6%). 1H NMR (CDCl3) δ 3.95 (s, 3H), 7.38 (d, 1H, J=1.5 Hz), 7.54 (m, 2H), 7.72 (d, 1H, J=7.5 Hz), 8.04 (d, 1H, J=7.5 Hz), 8.67 (d, 1H, J=1.5 Hz).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07084155B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-5203239c158e446e9e84abab6abb16bf
Quellennotizuspto-grants-2006_08