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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2209520생성일: 2026년 10월 26일

3-Nitrobenzaldehyde → 3-carboethoxy-2-trifluoromethyl-2-hydroxy-4-(3-nitrophenyl)-4,6,7,8-tetrahydro-5(1H)-quinolone

https://huagongshe.com/reaction/2209520

반응식

참여 물질

역할이름HCID투입량
반응물3-NitrobenzaldehydeHCID 7449—
반응물1,3-CyclohexanedioneHCID 10434—
반응물Ethyl 4,4,4-trifluoroacetoacetateHCID 67793—
반응물Ammonium AcetateHCID 517165—
용매EthanolHCID 702—
생성물3-carboethoxy-2-trifluoromethyl-2-hydroxy-4-(3-nitrophenyl)-4,6,7,8-tetrahydro-5(1H)-quinoloneHCID 19958905—

반응 단계

A stirred mixture of ethyl 4,4,4-trifluoroacetoacetate (6.00 mL), 1,3-cylohexanedione (4.65 g), 3-nitrobenzaldehyde (6.31 g), and ammonium acetate (6.57 g) in ethanol (350 mL) was heated at reflux for 4.5 hours. After removal of solvent the orange residue was treated diethyl ether, and the resulting precipitate was collected by filtration. The solid was triturated with hot diethyl ether, collected, and purified by chromatography (ethyl acetate) to yield 3-carboethoxy-2-trifluoromethyl-2-hydroxy-4-(3-nitrophenyl)-4,6,7,8-tetrahydro-5(1H)-quinolone (8.47 g) as a white solid. NMR: 0.85 (t,3, J=7.1, CH3), 1.86 (m,2, CH2), 2.07 (m,2, CH2), 2.27-2.44 (m,1, CH2), 2.57-2.72 (m,1, CH2), 2.75 (d,1, J=11.9, CH), 3.83 (m,2, CH2), 4.07 (d,1, J=11.4, CH), 7.30 (s,1, OH), 7.50 (m,1, Ar), 7.57 (m,1, Ar), 7.87 (m,1, Ar), 8.01 (m,1, Ar), 8.16 (s,1, NH); MS: m/z=428(M).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05455253
출처 데이터셋uspto-grants-1995_10
ORD IDord-0c72ab7d2c094e37ab87e0b6f36effa9
출처 메모uspto-grants-1995_10