Water → 1,5-Bis(3,4,5-trimethoxyphenyl)penta-1,4-dien-3-one

HRID 1085628

反応式

HRID 1085628 の反応式
[I-].C[N+]([CH2:6][CH2:7][C:8]([C:10]1[CH:15]=[C:14]([O:16][CH3:17])[C:13]([O:18][CH3:19])=[C:12]([O:20][CH3:21])[CH:11]=1)=O)(C)C.[C:22]([O:25][CH2:26][CH3:27])(=O)C.[OH2:28]>>[CH3:21][O:20][C:12]1[CH:11]=[C:10]([CH:8]=[CH:7][C:6]([CH:7]=[CH:8][C:10]2[CH:27]=[C:26]([O:25][CH3:22])[C:13]([O:18][CH3:19])=[C:14]([O:16][CH3:17])[CH:15]=2)=[O:28])[CH:15]=[C:14]([O:16][CH3:17])[C:13]=1[O:18][CH3:19]

参加物

4

実験手順

3-(N,N,N-trimethylammonio)-1-(3,4,5-trimethoxyphenyl)propan-1-one iodide (355.9 g, 0.87 mole) was suspended in a mixture of water (3.56 L) and of ethyl acetate (2.54 L) and refluxed with rapid stirring for 2-3 hours. The mixture was cooled and the pale yellow organic layer was removed. Fresh ethyl acetate (2 L) was added and the mixture was refluxed for 1 hour, and the process was repeated once again. The organic layers were combined, washed with brine, dried over anhydrous MgSO4, and evaporated to dryness to provide a yellow oil, which was crystallized from hexane/ether to give 3,4,5-trimethoxyphenylvinyl ketone (m.p. 45°-47° C.). 200 MHz 1H NMR (CDCl3): δ 3.94 (9H, s, 3 OCH3), 5.92 (1H, dd, J=1.5 Hz, J=9 Hz), 6.44 (1H, dd, J=1.5 Hz, J=1.5 Hz, J=16 Hz), 7.18 (1H, dd, J=16 Hz, J=9 Hz), 7.28 (2H, H2 and H6).

後処理

  1. temperaturerefluxed
  2. temperatureThe mixture was cooled
  3. customthe pale yellow organic layer was removed
  4. additionFresh ethyl acetate (2 L) was added
  5. temperaturethe mixture was refluxed for 1 hour
  6. washwashed with brine
  7. dry with materialdried over anhydrous MgSO4
  8. customevaporated to dryness
  9. customto provide a yellow oil, which
  10. customwas crystallized from hexane/ether

出典と根拠

ORDレコード
ord-1d344d6e311a4bccb1db48ae8e8a97d1
出典データセット
uspto-grants-1991_04
特許番号
US05010100

関連ノート

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