反応式
[C:1]1(=O)[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH2:3][CH2:2]1.Cl.[C:12]1(C)[CH:17]=[CH:16][C:15]([NH:18]N)=[CH:14][CH:13]=1>CCO.Cl>[CH:5]1[CH:6]=[CH:7][CH:8]=[C:9]2[C:4]=1[CH:3]=[C:2]1[C:16]3[CH:17]=[CH:12][CH:13]=[CH:14][C:15]=3[N:18]=[C:1]12参加物
5
実験手順
A mixture of 1-indanone (30.6 g, 232 mmol) and p-tolylhydrazine hydrochloride (37.0 g, 233 mmol) in EtOH (350 mL) and aqueous HCl (12 N, 18 mL) are heated to reflux for 90 min. The mixture is cooled and filtered, and the solid is washed with EtOH (600 mL) followed by 20% aqueous EtOH (400 mL) and finally hexanes (200 mL). The off-white solid is dried under vacuum (36.5 g, 72%).
後処理
- temperatureare heated
- temperatureto reflux for 90 min
- temperatureThe mixture is cooled
- filtrationfiltered
- washthe solid is washed with EtOH (600 mL)
- customThe off-white solid is dried under vacuum (36.5 g, 72%)
出典と根拠
- ORDレコード
- ord-3cb42a85ce85420d96f45874283b8385
- 出典データセット
- uspto-grants-2006_02
- 特許番号
- US06995216B2
関連ノート
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