반응식
Cl.[CH3:2][O:3][C:4]1[CH:5]=[C:6]([NH:10][NH2:11])[CH:7]=[CH:8][CH:9]=1.[N+:12]([CH2:15][C:16]([C:18]1C=CC=C[CH:19]=1)=O)([O-:14])=[O:13].[C:24]([O-])(=O)[CH3:25].[Na+].[C:29](O)(=O)[CH3:30]>O>[CH3:2][O:3][C:4]1[CH:5]=[C:6]([NH:10][N:11]=[C:29]([C:24]2[CH:25]=[CH:19][CH:18]=[CH:16][C:15]=2[N+:12]([O-:14])=[O:13])[CH3:30])[CH:7]=[CH:8][CH:9]=1참가 물질
6
실험 절차
A mixture of 3-methoxyphenylhydrazine hydrochloride (1.75 g), 2-nitroacetophenone (1.65 g), sodium acetate (0.82 g) and acetic acid (10 ml) was stirred at room temperature for 4 days. To the reaction mixture was added water, extracted with ethyl acetate. The extract was washed with water, brine, dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure to obtain the target compound (2.72 g).
후처리
- extractionextracted with ethyl acetate
- washThe extract was washed with water, brine
- dry with materialdried over anhydrous magnesium sulfate
- distillationThe solvent was distilled off under reduced pressure
출처 및 근거
- ORD 기록
- ord-573261e1a46940b09dc4e699d60da9d2
- 출처 데이터셋
- uspto-grants-2010_11
- 특허 번호
- US07842701B2
연결된 노트
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