Sodium hydride → N,N'-bis(n-butoxycarbonyl)-1,4-diketo-3,6-diphenylpyrrolo[3,4-c]pyrrole

HRID 52608노트

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HRID 52608 반응식
[O:1]=[C:2]1[C:6]2[C:7]([C:11]3[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=3)=[N:8][C:9](=[O:10])[C:5]=2[C:4]([C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)=[N:3]1.[H-].[Na+].Cl[C:26]([O:28][CH2:29][CH2:30][CH2:31][CH3:32])=[O:27]>O1CCCC1>[CH2:29]([O:28][C:26]([N:8]1[C:7]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)=[C:6]2[C:5](=[C:4]([C:17]3[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=3)[N:3]([C:26]([O:28][CH2:29][CH2:30][CH2:31][CH3:32])=[O:27])[C:2]2=[O:1])[C:9]1=[O:10])=[O:27])[CH2:30][CH2:31][CH3:32]

참가 물질

5

실험 절차

To a suspension of 0.5 g (0.00175 mol) of 1,4-diketo-3,6-diphenylpyrrolo[3,4-c]pyrrole in 17 ml of tetrahydrofuran are added, under argon, 0.28 g (0.007 mol) of solid sodium hydride. After stirring for 24 hours, 0.67 ml (0.007 mol) of n-butyl chloroformate are added and the suspension is stirred overnight. The mixture is filtered and the filtrate is concentrated under vacuum. The residue is taken up in water/diethyl ether, the organic phase is dried over MgSO4 and then concentrated under vacuum. The residue is taken up in n-hexane and the precipitated yellow powder is collected by filtration and washed with a minor amount of n-hexane, giving 0.62 g (73% of theory) of N,N'-bis(n-butoxycarbonyl)-1,4-diketo-3,6-diphenylpyrrolo[3,4-c]pyrrole as a yellow fluorescent powder.

후처리

  1. additionare added, under argon
  2. stirringthe suspension is stirred overnight
  3. filtrationThe mixture is filtered
  4. concentrationthe filtrate is concentrated under vacuum
  5. dry with materialthe organic phase is dried over MgSO4
  6. concentrationconcentrated under vacuum
  7. filtrationthe precipitated yellow powder is collected by filtration
  8. washwashed with a minor amount of n-hexane

출처 및 근거

ORD 기록
ord-66129e337d344ed5a9426bc67e89e139
출처 데이터셋
uspto-grants-1997_04
특허 번호
US05616725

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