Hydrogen Peroxide → 2-Propylpyridine 1-oxide

HRID 1421258

반응식

HRID 1421258 반응식
[CH2:1]([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][N:5]=1)[CH2:2][CH3:3].[OH:10]O>C(O)(=O)C>[CH2:1]([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][N+:5]=1[O-:10])[CH2:2][CH3:3]

참가 물질

4

반응 조건

온도
75 °C

실험 절차

To a solution of 2-n-propylpyridine (187.4 g, 1.505 mol) in 900 ml of acetic acid was added 149 ml of 35% aqueous hydrogen peroxide and the mixture was stirred and heated to 70-80° C. After three hours a further 104 ml of the hydrogen peroxide solution was added, and the mixture was maintained at the same temperature for an additional nine hours. The mixture was concentrated to about 300 ml in volume, 300 ml of water were added, and the mixture again concentrated as far as possible. The residue was made alkaline with anhydrous sodium carbonate, shaken with 750 ml of dichloromethane, and allowed to stand overnight. The resulting deposit of sodium carbonate and sodium acetate was removed by filtration. The filtrate was dried with magnesium sulfate, the solvent removed, and the residue distilled in vacuo. The yield of 2-n-propylpyridine-N-oxide, b.p. 120-140° C./9-15 mbar, was 176 g (81%). 1H-NMR (CDCl3, 200 MHz) δ: 1.05 (t, 3H), 1.80 (sext, 2H), 2.89 (t, 2H), 7.10-7.28 (m, 3H), 8.28 (d, 1H).

후처리

  1. temperaturethe mixture was maintained at the same temperature for an additional nine hours
  2. concentrationThe mixture was concentrated to about 300 ml in volume, 300 ml of water
  3. additionwere added
  4. concentrationthe mixture again concentrated as far as possible
  5. stirringshaken with 750 ml of dichloromethane
  6. customThe resulting deposit of sodium carbonate and sodium acetate was removed by filtration
  7. dry with materialThe filtrate was dried with magnesium sulfate
  8. customthe solvent removed
  9. distillationthe residue distilled in vacuo

출처 및 근거

ORD 기록
ord-acc02960aaea458089b8154be659abd7
출처 데이터셋
uspto-grants-2000_06
특허 번호
US06075036

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