반응식
[OH:1][C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:11]=1[N:10]=[C:9]([CH3:12])[CH:8]=[CH:7]2.[CH:13](=O)[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1>>[C:14]1([CH:13]=[CH:12][C:9]2[CH:8]=[CH:7][C:6]3[C:11](=[C:2]([OH:1])[CH:3]=[CH:4][CH:5]=3)[N:10]=2)[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1참가 물질
3
실험 절차
A mixture of 8-hydroxyquinaldine (10.02 g) and benzaldehyde (16.8 mL) is heated at reflux overnight. The reaction is cooled to room temperature and vacuum distilled. After the excess benzaldehyde has distilled off, the residue remaining in the flask is dissolved in hot 95% EtOH. Any undissolved material is filtered off. The EtOH filtrate is cooled slowly to give the product as light yellow crystals (5.17 g).
후처리
- temperatureis heated
- temperatureat reflux overnight
- distillationvacuum distilled
- distillationAfter the excess benzaldehyde has distilled off
- dissolutionis dissolved in hot 95% EtOH
- filtrationAny undissolved material is filtered off
- temperatureThe EtOH filtrate is cooled slowly
출처 및 근거
- ORD 기록
- ord-9769d0eac7db4f42a2218a50fc74dd7e
- 출처 데이터셋
- uspto-grants-2001_10
- 특허 번호
- US06310211B1
연결된 노트
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