Imidazole → 1-(4-Nitrophenyl)-1H-imidazole

HRID 1419775

반응식

HRID 1419775 반응식
[NH:1]1[CH:5]=[CH:4][N:3]=[CH:2]1.[H-].[Na+].F[C:9]1[CH:14]=[CH:13][C:12]([N+:15]([O-:17])=[O:16])=[CH:11][CH:10]=1.O>CN(C=O)C>[N:1]1([C:9]2[CH:14]=[CH:13][C:12]([N+:15]([O-:17])=[O:16])=[CH:11][CH:10]=2)[CH:5]=[CH:4][N:3]=[CH:2]1

참가 물질

6

실험 절차

To a stirred solution of imidazole (34.1 g, 0.50 mol) in DMF (300 ml) under Ar, was added portionwise, over 23 minutes, 60% NaH in oil (20.02 g, 0.50 mol). The mixture was then stirred at room temperature for 18 minutes before adding dropwise, over 40 minutes, a solution of 1-fluoro-4-nitrobenzene (70.62 g, 0.50 mol) in DMF (60 ml). The mixture was then stirred at room temperature overnight. Water (600 ml) was then added and the solid was filtered off, washed with water, then stirred in boiling ethyl acetate (400 ml), allowed to cool and filtered, washing the solid with more ethyl acetate (50 ml), then petroleum ether (250 ml). The filtrate, now containing more solid, was refiltered and washed with petroleum ether. The combined solids were dried in a vacuum desiccator overnight to give 90.14 g (95%) of the title compound as a yellow solid. δH (360 MHz, DMSO-d6) 7.19 (1H, t, J=1.1 Hz), 7.97-8.03 (3H, m), 8.38 (2H, d, J=9.2 Hz), 8.52 (1H, t).

후처리

  1. additionbefore adding dropwise, over 40 minutes
  2. stirringThe mixture was then stirred at room temperature overnight
  3. filtrationthe solid was filtered off
  4. washwashed with water
  5. stirringstirred
  6. temperatureto cool
  7. filtrationfiltered
  8. washwashing the solid with more ethyl acetate (50 ml)
  9. additionThe filtrate, now containing more solid
  10. washwashed with petroleum ether
  11. customThe combined solids were dried in a vacuum desiccator overnight

출처 및 근거

ORD 기록
ord-3244dd21988a4298beb37cc9f42fbe03
출처 데이터셋
uspto-grants-1999_03
특허 번호
US05889008

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