戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 55354作成日:2026年10月26日

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

https://huagongshe.com/reaction/55354

反応式

関与物質

役割名称HCID仕込み量
反応物Phosphorus trichlorideHCID 24387—
反応物Phosphorus oxychlorideHCID 24813—
反応物3-Ethoxycarbonyl-6,7-difluoro-1-hydroxy-2-oxoquinolineHCID 15294380—
反応物3-Ethoxycarbonyl-6,7-difluorocarbostyrilHCID 19957307—
溶媒1,2-DichloroethaneHCID 11—
生成物2-Chloro-3-ethoxycarbonyl-6,7-difluoroquinolineHCID 979546188%

反応条件

温度0 °C

反応手順

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%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05624933
出典データセットuspto-grants-1997_04
ORD IDord-2971a01b008d4de39939087bd95e35bf
出典メモuspto-grants-1997_04