戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1531695作成日:2026年10月26日

Diphenyl Ether → 3-Acetyl-7-chloro-8-ethoxycarbonyl-4-oxo-3,4-dihydro-1,10-phenanthroline

https://huagongshe.com/reaction/1531695

反応式

関与物質

役割名称HCID仕込み量
反応物Diphenyl EtherHCID 7583—
反応物Butanoic acid, 2-(ethoxymethylene)-3-oxo-, ethyl esterHCID 97734—
反応物8-Amino-4-chloro-3-ethoxycarbonylquinolineHCID 21250075—
溶媒Carbon TetrachlorideHCID 5943—
生成物3-Acetyl-7-chloro-8-ethoxycarbonyl-4-oxo-3,4-dihydro-1,10-phenanthrolineHCID 2125004529%

反応条件

温度90 °C

反応手順

A mixture of 8-amino-4-chloro-3-ethoxycarbonylquinoline (0.3 g) and ethyl 2-ethoxymethyleneacetoacetate (Annalen, 1897, 297, 16, 0.25 g) was heated at 90° C. for 2.5 hours. The mixture was cooled to ambient temperature and the resulting solid added to diphenyl ether at reflux. The mixture was refluxed for 45 minutes, and cooled to 60° C. The mixture was diluted with carbon tetrachloride (50 ml) and cooled to ambient temperature with stirring. The mixture was filtered and the solid so obtained purified by flash chromatography on silica using increasingly polar mixtures of methanol and chloroform. The product so obtained was recrystallised from methanol to give 3-acetyl-7-chloro-8-ethoxycarbonyl-4-oxo-3,4-dihydro-1,10-phenanthroline in 29% yield, mp 288-290° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06200974B1
出典データセットuspto-grants-2001_03
ORD IDord-fc9b0aec85c8416fb9bf4fc9609b7222
出典メモuspto-grants-2001_03