戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2269620作成日:2026年10月27日

Diethyl Malonate → Ethyl 1-benzyl-4-hydroxy-2-oxo-1,2-dihydroquinoline-3-carboxylate

https://huagongshe.com/reaction/2269620

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl MalonateHCID 7761—
反応物Sodium hydrideHCID 24758—
反応物N-Benzylisatoic anhydrideHCID 520756—
反応物HCID 178418361HCID 178418361—
溶媒DimethylformamideHCID 6228—
生成物Ethyl 1-benzyl-4-hydroxy-2-oxo-1,2-dihydroquinoline-3-carboxylateHCID 5471183768.7%

反応条件

温度80 °C

反応手順

In a solution of 4.50 g of diethyl malonate in 20 ml of N,N-dimethylformamide was gradually added 1.10 g of 62.4% sodium hydride at room temperature, and stirring was continued at room temperature until hydrogen evolution ceased. The reaction solution was heated to 80° C., and a solution of 6.70 g of N-benzylisatoic anhydride in 20 ml of N,N-dimethylformamide was added dropwise. After the addition, the reaction mixture was stirred under heating at 120° C. for 7 hours. After cooling to room temperature, the reaction mixture was poured into ice water and washed with ethyl acetate. The aqueous phase was made acidic with 1 N hydrochloric acid, and extracted with ethyl acetate. The organic phase was washed with a saturated aqueous sodium chloride solution, and dried over anhydrous magnesium sulfate. After removal of the drying agent by filtration, the filtrate was concentrated under reduced pressure. The residue was crystallized from ethanol to give 5.88 g of ethyl 1-benzyl-4-hydroxy-1,2-dihydro-2-oxoquinoline-3-carboxylate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06329525B1
出典データセットuspto-grants-2001_12
ORD IDord-7ea00b8b48ac4a6e87e7014f410351f6
出典メモuspto-grants-2001_12