反応式
[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]=1参加物
3
実験手順
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).
後処理
- 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
出典と根拠
- ORDレコード
- ord-9769d0eac7db4f42a2218a50fc74dd7e
- 出典データセット
- uspto-grants-2001_10
- 特許番号
- US06310211B1
関連ノート
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