4,4'-Dimethoxybenzophenone → Tas-301

HRID 1600876ノート

反応式

HRID 1600876 の反応式
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH2:3][C:2]1=[O:10].[CH3:11][O:12][C:13]1[CH:28]=[CH:27][C:16]([C:17]([C:19]2[CH:24]=[CH:23][C:22]([O:25][CH3:26])=[CH:21][CH:20]=2)=O)=[CH:15][CH:14]=1.[H-].[Na+].[H][H].[Cl-].[NH4+]>O1CCCC1>[CH3:26][O:25][C:22]1[CH:21]=[CH:20][C:19]([C:17]([C:16]2[CH:27]=[CH:28][C:13]([O:12][CH3:11])=[CH:14][CH:15]=2)=[C:3]2[C:4]3[C:9](=[CH:8][CH:7]=[CH:6][CH:5]=3)[NH:1][C:2]2=[O:10])=[CH:24][CH:23]=1

参加物

7

実験手順

10.0 g of oxindole was dissolved in 100 ml tetrahydrofuran, and 21.8 g of 4,4'-dimethoxybenzophenone was added thereto at room temperature. Subsequently, the temperature of the reaction was brought to 0° C. 9.0 g of 60% sodium hydride was added, and when generation of hydrogen ceased, the reaction mixture was refluxed with heat for 12 hours. After completion of reaction, the reaction mixture was cooled. Saturated aqueous ammonium chloride solution was added, followed by extraction with ethyl acetate. The extract was washed with water and saturated brine, dried over sodium sulfate, and then evaporated. The resultant crude product was recrystallized from methanol, to thereby obtain 22.8 g (yield 85%) of the title compound in yellow crystals (Crystal 1). The melting point and elementary analysis data are shown in Table 1, and NMR and MS spectrum data are shown in Table 2. Also, the IR spectrum chart of the compound is shown in FIG. 1.

後処理

  1. customat room temperature
  2. customwas brought to 0° C
  3. temperaturethe reaction mixture was refluxed
  4. temperaturewith heat for 12 hours
  5. customAfter completion of reaction
  6. temperaturethe reaction mixture was cooled
  7. extractionfollowed by extraction with ethyl acetate
  8. washThe extract was washed with water and saturated brine
  9. dry with materialdried over sodium sulfate
  10. customevaporated
  11. customThe resultant crude product was recrystallized from methanol

出典と根拠

ORDレコード
ord-d8c84c9e640645258b72d54d9a6c6ad1
出典データセット
uspto-grants-1999_11
特許番号
US05977130

反応ノート

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