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HRID 55354Erstellt: 25. Oktober 2026

Phosphorus trichloride → 2-Chloro-3-ethoxycarbonyl-6,7-difluoroquinoline

https://huagongshe.com/reaction/55354

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhosphorus trichlorideHCID 24387—
EduktPhosphorus oxychlorideHCID 24813—
Edukt3-Ethoxycarbonyl-6,7-difluoro-1-hydroxy-2-oxoquinolineHCID 15294380—
Edukt3-Ethoxycarbonyl-6,7-difluorocarbostyrilHCID 19957307—
Lösungsmittel1,2-DichloroethaneHCID 11—
Produkt2-Chloro-3-ethoxycarbonyl-6,7-difluoroquinolineHCID 979546188%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

A mixture of 3-ethoxycarbonyl-6,7-difluoro-1-hydroxy-2-oxoquinoline (25 g at a concentration of 75 mol %, equivalent to 69.65 mmol), 3-ethoxycarbonyl6,7-difluoro-2-oxoquinoline (25 g at a concentration of 5 mol %, equivalent to 4.9 mmol), phosphorus trichloride (59.6 g, equivalent to 433.5 mmol) and phosphoryl chloride (15.05 g, equivalent to 98.05 mmol) in 1,2-dichloroethane (170 cm3) is heated at reflux for 3 hours. After cooling to 0° C., the reaction mixture is poured onto slushed ice (250 g of ice +250 g of water at 0° C.) and left to separate overnight. The organic phase is washed with saturated NaHCO3 solution (100 cm3), followed by water (100 cm3), and then concentrated to dryness in order to obtain 19.8 g of 3-ethoxycarbonyl-6,7-difluoro-2-chloroquinoline of 90% assay (HPLC), equivalent to a yield of 88%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05624933
Quelldatensatzuspto-grants-1997_04
ORD IDord-2971a01b008d4de39939087bd95e35bf
Quellennotizuspto-grants-1997_04