反応式
[CH3:1][O:2][C:3]1[CH:4]=[C:5](/[CH:11]=[C:12](/[C:16]2[CH:21]=[CH:20][C:19]([OH:22])=[CH:18][CH:17]=2)\[C:13]([OH:15])=[O:14])[CH:6]=[C:7]([O:9][CH3:10])[CH:8]=1.[CH3:23]O>S(=O)(=O)(O)O>[CH3:23][O:14][C:13](=[O:15])/[C:12](/[C:16]1[CH:17]=[CH:18][C:19]([OH:22])=[CH:20][CH:21]=1)=[CH:11]\[C:5]1[CH:6]=[C:7]([O:9][CH3:10])[CH:8]=[C:3]([O:2][CH3:1])[CH:4]=1参加物
実験手順
Concentrated sulfuric acid (10 drops) was added to a stirred methanol suspension of thoroughly dried 19 (0.60 g, 2.0 mmol) under argon and heated at reflux for 18 h. Methanol was evaporated under reduced pressure, residue was taken up in ethyl acetate (20 mL) and washed with water (20 mL), saturated aqueous Na HCO3 (10 mL) and brine (10 mL). The organic layer was dried on anhydrous magnesium sulfate, filtered and the solvent was evaporated. The crude product obtained was purified by chromatography over silica gel and eluted with hexane-ethyl acetate (7:3) to yield 20 as white solid (0.24 g, 35%): 1HNMR (400 MHz, CDCl3) δ 7.26 (d, J=8.4 Hz, 2H), 6.82 (s, 1H), 6.76 (d, J=8.4 Hz, 2H), 6.45 (d, J=2.0 Hz, 2H), 6.34 (t, J=2.0 Hz, 1H), 4.97 (s, 1H), 3.73(s, 3H), 3.72(s, 6H).
後処理
- temperatureheated
- temperatureat reflux for 18 h
- customMethanol was evaporated under reduced pressure, residue
- washwashed with water (20 mL), saturated aqueous Na HCO3 (10 mL) and brine (10 mL)
- dry with materialThe organic layer was dried on anhydrous magnesium sulfate
- filtrationfiltered
- customthe solvent was evaporated
- customThe crude product obtained
- customwas purified by chromatography over silica gel
- washeluted with hexane-ethyl acetate (7:3)
出典と根拠
- ORDレコード
- ord-0dc1d8b0f8614c3d86197a8820699e1f
- 出典データセット
- uspto-grants-2008_08
- 特許番号
- US07407978B2
関連ノート
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