Acetyl chloride → HCID 53740391、化合物
反応式
[N:1]1([CH:6]([C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)[C:7]2[CH:12]=[CH:11][C:10]([NH2:13])=[C:9]([N+:14]([O-:16])=[O:15])[CH:8]=2)[CH:5]=[CH:4][N:3]=[CH:2]1.[C:23](Cl)(=[O:25])[CH3:24]>C(O)(=O)C>[N:1]1([CH:6]([C:17]2[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=2)[C:7]2[CH:12]=[CH:11][C:10]([NH:13][C:23](=[O:25])[CH3:24])=[C:9]([N+:14]([O-:16])=[O:15])[CH:8]=2)[CH:5]=[CH:4][N:3]=[CH:2]1参加物
4
実験手順
(a-4) A mixture of 1.45 parts of 4-[(1H-imidazol-1-yl)phenylmethyl]-2-nitrobenzenamine, 0.78 parts of acetyl chloride and 25 parts of acetic acid was stirred over weekend at room temperature. The methanol layer was removed in vacuo and the residue was taken up in water and dichloromethane. After treatment with ammonium hydroxide, the dichloromethane layer was dried, filtered and evaporated, yielding 1.6 parts (95%) of N-[4-[(1H-imidazol-1-yl)phenylmethyl]-2-nitrophenyl]-acetamide as a residue (int. 127).