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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 3-Nitrobenzaldehyde | HCID 7449 | — |
| 반응물 | 1,3-Cyclohexanedione | HCID 10434 | — |
| 반응물 | Ethyl 4,4,4-trifluoroacetoacetate | HCID 67793 | — |
| 반응물 | Ammonium Acetate | HCID 517165 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | 3-carboethoxy-2-trifluoromethyl-2-hydroxy-4-(3-nitrophenyl)-4,6,7,8-tetrahydro-5(1H)-quinolone | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05455253 |
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| 출처 데이터셋 | uspto-grants-1995_10 |
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| ORD ID | ord-0c72ab7d2c094e37ab87e0b6f36effa9 |
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| 출처 메모 | uspto-grants-1995_10 |
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