Hydrogen Peroxide → Pyridine, 3-ethyl-, 1-oxide

HRID 1913756

반응식

HRID 1913756 반응식
[CH2:1]([C:3]1[CH:4]=[N:5][CH:6]=[CH:7][CH:8]=1)[CH3:2].OO.C(=O)([O-])[O-:12].[Na+].[Na+]>C(O)(=O)C>[CH2:1]([C:3]1[CH:4]=[N+:5]([O-:12])[CH:6]=[CH:7][CH:8]=1)[CH3:2]

참가 물질

5

반응 조건

온도
80 °C

실험 절차

A mixture of 10.0 g of 3-ethylpyridine, 60 ml of acetic acid and 12 ml of 30% hydrogen peroxide solution was stirred while heating at 80° C. for 2.5 hours. To the reaction mixture, 7 ml of 30% hydrogen peroxide solution was added, and the reaction mixture was stirred while heating at 80° C. for further seven hours. The reaction mixture was cooled to room temperature, and sodium carbonate was added to the reaction mixture in small portions. The reaction mixture was filtered, and washed with ethyl acetate. The resultant filtrate was washed with a saturated aqueous solution of sodium hydrogensulfite and a saturated sodium chloride solution, dried over anhydrous water sodium carbonate. Activated carbon was added, followed by filtration through Celite™. The filtrate was concentrated under reduced pressure to give 6.0 g of 3-ethylpyridine N-oxide.

후처리

  1. stirringthe reaction mixture was stirred
  2. temperaturewhile heating at 80° C. for further seven hours
  3. temperatureThe reaction mixture was cooled to room temperature
  4. filtrationThe reaction mixture was filtered
  5. washwashed with ethyl acetate
  6. washThe resultant filtrate was washed with a saturated aqueous solution of sodium hydrogensulfite
  7. dry with materiala saturated sodium chloride solution, dried over anhydrous water sodium carbonate
  8. additionActivated carbon was added
  9. filtrationfollowed by filtration through Celite™
  10. concentrationThe filtrate was concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-1b014344b2004d42b29526779c1bbf68
출처 데이터셋
uspto-grants-2013_12
특허 번호
US08609705B2

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