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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 844523생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/844523

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl MalonateHCID 7761—
반응물Sodium hydrideHCID 24758—
반응물N-Benzylisatoic anhydrideHCID 520756—
반응물HCID 178418361HCID 178418361—
용매DimethylformamideHCID 6228—
생성물Ethyl 1-benzyl-4-hydroxy-2-oxo-1,2-dihydroquinoline-3-carboxylateHCID 5471183768.7%

반응 조건

온도80 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06380384B1
출처 데이터셋uspto-grants-2002_04
ORD IDord-c999211ed9f44416bb7d7863c806ce2c
출처 메모uspto-grants-2002_04