Nitrobenzene → 1,4-Benzenediamine, N-(4-nitrophenyl)-

HRID 54729

반응식

HRID 54729 반응식
[N+:1]([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1)([O-:3])=[O:2].[C:10]1([NH2:17])[CH:15]=[CH:14][C:13]([NH2:16])=[CH:12][CH:11]=1.[OH2:18].O.O.O.O.[OH-].C[N+:25]([CH3:28])(C)[CH3:26]>CS(C)=O>[N:1]([C:4]1[CH:9]=[CH:8][C:7]([NH:16][C:13]2[CH:14]=[CH:15][C:10]([NH2:17])=[CH:11][CH:12]=2)=[CH:6][CH:5]=1)=[O:3].[N+:1]([C:4]1[CH:5]=[CH:6][C:26]([NH:25][C:28]2[CH:8]=[CH:9][C:4]([NH:16][C:13]3[CH:14]=[CH:15][C:10]([N:17]=[O:18])=[CH:11][CH:12]=3)=[CH:5][CH:6]=2)=[CH:8][CH:9]=1)([O-:3])=[O:2].[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([NH:16][C:13]2[CH:14]=[CH:15][C:10]([NH2:17])=[CH:11][CH:12]=2)=[CH:6][CH:5]=1)([O-:3])=[O:2]

참가 물질

7

실험 절차

Nitrobenzene (2 ml, 0.02 mole) was added via a syringe to a stirring solution containing 1.08 g (0.01 mole) of 1,4-phenylenediamine, 3.6 g (0.02 mole) of tetramethylammonium hydroxide pentahydrate in 2 ml of dimethylsulfoxide under nitrogen at 70° C. The solution was stirred at such condition for 4 hours. An aliquot was taken out for LC, MS, LC-MS analyses. N,N'-(4-nitrosophenyl)-1,4-phenylenediamine, N-(4-nitrophenyl)-N'-(4-nitrosophenyl)-1,4-phenylenediamine and N,N'-(4-nitrophenyl)-1,4-phenylenediamine were obtained.

출처 및 근거

ORD 기록
ord-e63fd5b95f1b4e59b5d2758ec5cd15e6
출처 데이터셋
uspto-grants-1997_04
특허 번호
US05623088

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