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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 39730Erstellt: 24. Oktober 2026

4-Chloro-7-(trifluoromethyl)quinoline → 4-Chloro-1-oxo-7-(trifluoromethyl)-1lambda~5~-quinoline

https://huagongshe.com/de/reaction/39730

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Chloro-7-(trifluoromethyl)quinolineHCID 67668—
Eduktm-Chloroperbenzoic acidHCID 70297—
EduktSodium BicarbonateHCID 516892—
LösungsmittelChloroformHCID 6212—
Produkt4-Chloro-1-oxo-7-(trifluoromethyl)-1lambda~5~-quinolineHCID 23128133—

Reaktionsschritte

To 14 mL of a chloroform solution containing 0.90 g of 4-chloro-7-trifluoromethylquinoline, 1.04 g of m-chloroperbenzoic acid was added, and the mixture was stirred at room temperature for 3.5 hours. The reaction mixture was added with 15 mL of an aqueous saturated sodium hydrogen carbonate solution. The organic layer was separated, and the aqueous layer was extracted with chloroform. The organic layer and the extract were combined, the resultant solution was washed with an aqueous saturated sodium chloride solution, and dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure to obtain a yellow solid, 4-chloro-7-trifluoromethylquinoline N-oxide.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08524738B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-0c9d7f38499840a9bd74ad95e8a955b4
Quellennotizuspto-grants-2013_09