참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethanol | HCID 702 | — |
| 반응물 | 1,3-Cyclohexanedione | HCID 10434 | — |
| 반응물 | 4-(4-Methylphenyl)-3-buten-2-one | HCID 107388 | — |
| 반응물 | Ammonium Acetate | HCID 517165 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 용매 | Ethyl acetate hexane | HCID 21226206 | — |
| 생성물 | 2-Methyl-4-(4-methylphenyl)-4,6,7,8-tetrahydro-5(1H)-quinolone | HCID 19958930 | 25.3% |
반응 단계
A mixture of 4-(4-methyphenyl)-3-butene-2-one (5.0 g), 1,3-cyclohexanedione (3.66 g), ammonium acetate (3.61 g) and 100 mL of ethanol were heated at reflux overnight and then cooled to room temperature. The solvent was evaporated and the residue was partitioned between water and ethyl acetate. The organic layer was dried, filtered, and evaporated to obtain an amber oil. Chromatography, with hexane:ethyl acetate (1:1) as the eluent, and trituration from ether provided the title compound as an off-white solid (2.0 g); mp 196°-198° C.; NMR: 1.73 (s,3, CH3), 1.87-1.98 (m,2, CH2), 2.14-2.16 (m,2, CH2), 2.22 (s,3, CH3), 2.43-2.49 (m,2, CH2) 4.34 (d,1, CH), 4.57 (d,1, CH), 7.01 (s,4, Ar), 8.40 (s,1, NH); (CI, CH4) MS: m/z=254(M+1). Analysis for C17H19NO: Calculated: C, 80.60; H, 7.56; N, 5.53; Found: C, 80.24; H, 7.68; N, 5.36.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US05622964 |
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| 출처 데이터셋 | uspto-grants-1997_04 |
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| ORD ID | ord-5813a68cf35f46dd87204589308f1001 |
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| 출처 메모 | uspto-grants-1997_04 |
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