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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 69045Erstellt: 23. Oktober 2026

Hydrogen Peroxide → 3-Bromoquinolin-2-ol

https://huagongshe.com/de/reaction/69045

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrogen PeroxideHCID 784—
EduktPotassium CarbonateHCID 11430—
Edukt3-BromoquinolineHCID 21413—
EduktSodium SulfiteHCID 24437—
KatalysatorHCID 178477782HCID 178477782—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
Produkt3-Bromoquinolin-2-olHCID 268338—

Reaktionsschritte

Hydrogen peroxide solution (5.9 ml) was added to a THF solution (16 ml) of methyltrioxorhenium (VII) (24 mg). The mixture was stirred for 10 minutes at room temperature. 3-Bromoquinoline (4.0 g) was added thereto, and the mixture was stirred at room temperature for four days. Ethyl acetate (20 ml) was added to the reaction mixture. 20% Sodium sulfite aqueous solution (30 ml) was added slowly to the mixture under ice cooling. The mixture was stirred at room temperature. The organic layer was condensed to a half volume under reduced pressure. Ethyl acetate (20 ml) and 15% potassium carbonate aqueous solution (19 ml) were added thereto, and the organic layer was extracted. 15% Potassium carbonate aqueous solution (19 ml) of p-toluenesulfonyl chloride (4 g) were added thereto. The mixture was stirred for 10 minutes at room temperature. The generated insoluble matter was separated, washed with ethyl acetate, water, and then with ether, and dried to give the title compound (3.2 g) as a white powder.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08822453B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-4619ec1e0624416bb44eb940d1a9c089
Quellennotizuspto-grants-2014_09