Sodium Sulfite → 4-(4-Nitrophenyl)-morpholin-3-ON

HRID 18525

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HRID 18525 반응식
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([N:10]2[CH2:15][CH2:14][O:13][CH2:12][CH2:11]2)=[CH:6][CH:5]=1)([O-:3])=[O:2].[Mn]([O-])(=O)(=O)=[O:17].[K+].[O-]S([O-])=O.[Na+].[Na+]>C(Cl)Cl.[Cl-].C([N+](CC)(CC)CC)C1C=CC=CC=1.O>[N+:1]([C:4]1[CH:5]=[CH:6][C:7]([N:10]2[CH2:15][CH2:14][O:13][CH2:12][C:11]2=[O:17])=[CH:8][CH:9]=1)([O-:3])=[O:2]

참가 물질

7

실험 절차

To a solution of 10 g 4-(4-Nitro-phenyl)-morpholine in 200 mL DCM, 32 g Benzyl-triethyl-ammonium chloride and 22.7 g potassium permanganate (325 mesh) were cautiously added at RT. After stirring for 1 h at RT the reaction mixture was heated to reflux for 10 h. Then a solution of 95 g Na2SO3 in 450 mL water were added under ice cooling and vigourous stirring. The mixture was filtered trough a pad of celite and the filtrate was concentrated under reduced pressure. The yellow solid was stirred with 250 mL water and the precipitated product was collected by filtration. This crude product was purified by chromatography on silica gel eluting with a gradient of DCM/MeOH 100%->50%. The fractions containing the product were combined and the solvent evaporated under reduced pressure. Yield: 2.6 g.

후처리

  1. temperaturewas heated
  2. temperatureto reflux for 10 h
  3. filtrationThe mixture was filtered trough a pad of celite
  4. concentrationthe filtrate was concentrated under reduced pressure
  5. stirringThe yellow solid was stirred with 250 mL water
  6. filtrationthe precipitated product was collected by filtration
  7. customThis crude product was purified by chromatography on silica gel eluting with a gradient of DCM/MeOH 100%->50%
  8. additionThe fractions containing the product
  9. customthe solvent evaporated under reduced pressure

출처 및 근거

ORD 기록
ord-685845651df844258e0bca4fa4eb1884
출처 데이터셋
uspto-grants-2010_06
특허 번호
US07741341B2

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