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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 55354Generated: October 25, 2026

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

https://huagongshe.com/reaction/55354

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus trichlorideHCID 24387—
ReactantPhosphorus oxychlorideHCID 24813—
Reactant3-Ethoxycarbonyl-6,7-difluoro-1-hydroxy-2-oxoquinolineHCID 15294380—
Reactant3-Ethoxycarbonyl-6,7-difluorocarbostyrilHCID 19957307—
Solvent1,2-DichloroethaneHCID 11—
Product2-Chloro-3-ethoxycarbonyl-6,7-difluoroquinolineHCID 979546188%

Reaction Conditions

Temperature0 °C

Reaction Steps

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%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05624933
Source datasetuspto-grants-1997_04
ORD IDord-2971a01b008d4de39939087bd95e35bf
Source noteuspto-grants-1997_04