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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 503988Erstellt: 27. Oktober 2026

Dimethylformamide → 1-(4-Chlorobenzyl)-2-oxo-1,2-dihydroquinoline-3-carboxaldehyde

https://huagongshe.com/reaction/503988

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktSodium hydrideHCID 24758—
Edukt1-(Bromomethyl)-4-chlorobenzeneHCID 69329—
Edukt2-Hydroxyquinoline-3-carbaldehydeHCID 589334—
LösungsmittelWaterHCID 962—
LösungsmittelEthyl AcetateHCID 8857—
Produkt1-(4-Chlorobenzyl)-2-oxo-1,2-dihydroquinoline-3-carboxaldehydeHCID 8661391674,5%

Reaktionsschritte

Sodium hydride (60% in oil) (1.3 g) was added at 0° C. to a DMF solution (50 ml) of 2-oxo-1,2-dihydroquinoline-3-carboxaldehyde (5.13 g), followed by stirring for 30 minutes. 4-chlorobenzyl bromide (7.0 g) was added, and the resulting mixture was stirred at room temperature overnight. Water was added to the reaction mixture, extraction with ethyl acetate was performed, and the extract was dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:n-hexane=1:10→1:4). The purified product was recrystallized from a chloroform-diisopropyl ether mixed solvent to thereby obtain 6.57 g (yield: 72%) of 1-(4-chlorobenzyl)-2-oxo-1,2-dihydroquinoline-3-carboxaldehyde as a white powder.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07777038B2
Quelldatensatzuspto-grants-2010_08
ORD IDord-9e7a01cee91b48e1bf118eee2345eedd
Quellennotizuspto-grants-2010_08