4-Methyl-1,7-diphenyl-1,6-heptadiene-3,5-dione → 4-Methyl-1,7-diphenylheptane-3,5-dione
反応式
[CH3:1][CH:2]([C:13](=[O:22])[CH:14]=[CH:15][C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)[C:3](=[O:12])[CH:4]=[CH:5][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1>[Pd].C(OCC)(=O)C>[CH3:1][CH:2]([C:3](=[O:12])[CH2:4][CH2:5][C:6]1[CH:7]=[CH:8][CH:9]=[CH:10][CH:11]=1)[C:13](=[O:22])[CH2:14][CH2:15][C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1参加物
実験手順
4-Methyl-1,7-diphenyl-1,6-hetpadiene-3,5-dione (6b, 0.96 g, 3.3 mmol) and palladium on activated carbon (0.25 g, 10%) were combined in ethyl acetate (50 ml). The mixture was placed under a hydrogen atmosphere (60 psi) on a Parr apparatus for 2 hr at room temperature. The resulting mixture was filtered through celite and the filtrate was washed with saturated sodium chloride, dried over magnesium sulfate, filtered and evaporated to afford an oil. The crude oil was twice chromatographed on silica gel with ethyl acetate/hexane to give an oil. The oil was distilled bulb to bulb to give 0.71 g (73%) of a clear oil; 1H NMR: δ enol form: 1.66 (s, 3H), 2.73 (m, 8H), 7.17 (m, 10H); keto form: 1.20 (d, 3H, J=7.2 Hz), 2.73 (m, 8H), 3.55 (q, 1H, J=7.0 Hz), 7.17 (m, 10H); 13C NMR: δ 12.3, 29.3, 31.0, 37.6, 42.8, 60.9, 104.2, 125.9, 128.1, 128.2, 140.4, 140.8, 174.6, 191.5, 205.6; Exact mass calcd for C20H22O2: 294.1620, observed (M+H) 295.1693.
後処理
- customfor 2 hr
- customat room temperature
- filtrationThe resulting mixture was filtered through celite
- washthe filtrate was washed with saturated sodium chloride
- dry with materialdried over magnesium sulfate
- filtrationfiltered
- customevaporated
- customto afford an oil
- customThe crude oil was twice chromatographed on silica gel with ethyl acetate/hexane
- customto give an oil
- distillationThe oil was distilled bulb to bulb
出典と根拠
- ORDレコード
- ord-5333404f7c1748e38f8ab1189533bda1
- 出典データセット
- uspto-grants-2015_11
- 特許番号
- US09187397B2
反応ノート
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