Chloroform → 8-(3-Amino-2,6-dimethylbenzyloxy)-2-methylquinoline
반응식
[CH3:1][C:2]1[C:20]([N+:21]([O-])=O)=[CH:19][CH:18]=[C:17]([CH3:24])[C:3]=1[CH2:4][O:5][C:6]1[CH:7]=[CH:8][CH:9]=[C:10]2[C:15]=1[N:14]=[C:13]([CH3:16])[CH:12]=[CH:11]2.O.NN.C(Cl)(Cl)Cl>CO>[NH2:21][C:20]1[C:2]([CH3:1])=[C:3]([C:17]([CH3:24])=[CH:18][CH:19]=1)[CH2:4][O:5][C:6]1[CH:7]=[CH:8][CH:9]=[C:10]2[C:15]=1[N:14]=[C:13]([CH3:16])[CH:12]=[CH:11]2참가 물질
실험 절차
To a suspension of 8-(2,6-dimethyl-3-nitrobenzyloxy)-2-methylquinoline (2.34 g), ferric chloride (70.6 mg) and carbon (70.6 mg) in methanol (35 ml) was added hydrazine monohydrate (1.09 g) at 65° C., and the mixture was refluxed for 2 hours. Methanol (20 ml) was added thereto, and the mixture was refluxed for 1 hour. After cooling chloroform was added thereto, and the resulting precipitates were filtered off. The filtrate was concentrated and the residue was dissolved in chloroform. The solution was washed with saturated sodium bicarbonate solution, water and brine, dried over magnesium sulfate and concentrated. The residue was crystallized with ethyl acetate to give 8-(3-amino-2,6-dimethylbenzyloxy)-2-methylquinoline (1.67 g) as a pale brown crystal.
후처리
- temperaturethe mixture was refluxed for 2 hours
- temperaturethe mixture was refluxed for 1 hour
- additionwas added
- customthe resulting precipitates
- filtrationwere filtered off
- concentrationThe filtrate was concentrated
- dissolutionthe residue was dissolved in chloroform
- washThe solution was washed with saturated sodium bicarbonate solution, water and brine
- dry with materialdried over magnesium sulfate
- concentrationconcentrated
- customThe residue was crystallized with ethyl acetate
출처 및 근거
- ORD 기록
- ord-71dd8e115c8a4e3f8d7478c62fde2609
- 출처 데이터셋
- uspto-grants-2002_02
- 특허 번호
- US06344462B1
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