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HRID 331208作成日:2026年10月26日

Phosphorus oxychloride → 4-Chloro-6,7-dimethoxyquinoline

https://huagongshe.com/reaction/331208

反応式

関与物質

役割名称HCID仕込み量
反応物Phosphorus oxychlorideHCID 24813—
反応物HCID 178486804HCID 178486804—
溶媒AcetonitrileHCID 6342—
生成物4-Chloro-6,7-dimethoxyquinolineHCID 45961073.4%

反応条件

温度65 °C

反応手順

A reactor was charged sequentially with 6,7-dimethoxy-quinoline-4-ol (1 L, 10.0 kg) and acetonitrile (64.0 L). The resulting mixture was heated to approximately 65° C. and phosphorus oxychloride (POCl3, 50.0 kg) was added. After the addition of POCl3, the temperature of the reaction mixture was raised to approximately 80° C. The reaction was deemed complete (approximately 9.0 hours) when <2% of the starting material remained (in process high-performance liquid chromatography [HPLC] analysis). The reaction mixture was cooled to approximately 10° C. and then quenched into a chilled solution of dichloromethane (DCM, 238.0 kg), 30% NH4OH (135.0 kg), and ice (440.0 kg). The resulting mixture was warmed to approximately 14° C., and phases were separated. The organic phase was washed with water (40.0 kg) and concentrated by vacuum distillation with the removal of solvent (approximately 190.0 kg). Methyl-t-butyl ether (MTBE, 50.0 kg) was added to the batch, and the mixture was cooled to approximately 10° C., during which time the product crystallized out. The solids were recovered by centrifugation, washed with n-heptane (20.0 kg), and dried at approximately 40° C. to afford the title compound (8.0 kg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08877776B2
出典データセットuspto-grants-2014_11
ORD IDord-d83b21da9c4c424f8a970bcfe82e8c35
出典メモuspto-grants-2014_11