Methanol → HCID 15541463、化合物

HRID 2217616

反応式

HRID 2217616 の反応式
[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

4

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

  1. temperatureheated
  2. temperatureat reflux for 18 h
  3. customMethanol was evaporated under reduced pressure, residue
  4. washwashed with water (20 mL), saturated aqueous Na HCO3 (10 mL) and brine (10 mL)
  5. dry with materialThe organic layer was dried on anhydrous magnesium sulfate
  6. filtrationfiltered
  7. customthe solvent was evaporated
  8. customThe crude product obtained
  9. customwas purified by chromatography over silica gel
  10. 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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