2-Benzyloxy-5-nitroiodobenzene → 4-(Benzyloxy)-3-iodobenzenamine

HRID 565379ノート

反応式

HRID 565379 の反応式
[CH2:1]([O:8][C:9]1[CH:14]=[CH:13][C:12]([N+:15]([O-])=O)=[CH:11][C:10]=1[I:18])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1>O.C(O)(=O)C.[Fe]>[CH2:1]([O:8][C:9]1[CH:14]=[CH:13][C:12]([NH2:15])=[CH:11][C:10]=1[I:18])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

参加物

5

反応条件

温度
80 °C

実験手順

Iron powder (12.5 g, 224 mmol) was added to a suspension of 2-benzyloxy-5-nitroiodobenzene (Description 13; 10 g, 28 mmol) in water (300 ml) and acetic acid (75 ml) and the mixture was stirred at 80° C. for 12 hours. The mixture was allowed to cool to room temperature and filtered through Hyflo™, washing with 4:1 water:acetic acid and ethyl acetate. The filtrate was extracted with ethyl acetate, and the organic extract was evaporated under reduced pressure. Saturated aqueous sodium hydrogen carbonate was added and the mixture was extracted with ethyl acetate. The organic extract was washed with brine, dried (MgSO4), and the solvent was evaporated under reduced pressure to give the title compound as a brown oil (9 g, 99% yield). 1H NMR (360 MHz, CDCl3) δ 7.49−7.47 (2H, m), 7.40−7.28 (3H, m), 7.19 (1H, d, J 2.4 Hz), 6.70 (1H, d, J 8.6 Hz), 6.62 (1H, dd, J 2.4, 8.6 Hz), and 5.04 (2H, s). m/z (ES+) 326 (M+1)+.

後処理

  1. temperatureto cool to room temperature
  2. filtrationfiltered through Hyflo™
  3. washwashing with 4:1 water
  4. extractionThe filtrate was extracted with ethyl acetate
  5. extractionthe organic extract
  6. customwas evaporated under reduced pressure
  7. additionSaturated aqueous sodium hydrogen carbonate was added
  8. extractionthe mixture was extracted with ethyl acetate
  9. extractionThe organic extract
  10. washwas washed with brine
  11. dry with materialdried (MgSO4)
  12. customthe solvent was evaporated under reduced pressure

出典と根拠

ORDレコード
ord-5f26c52a30024988b632e1744e62b7be
出典データセット
uspto-grants-2001_01
特許番号
US06172077B2

反応ノート

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