反応式
[C:1](#[N:10])[CH:2]=[CH:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.[NH3:11].CO>CCO>[C:4]1(/[CH:3]=[CH:2]/[C:1](=[NH:11])[NH2:10])[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1参加物
4
反応条件
- 温度
- 0 °C
実験手順
Cinnamonitrile (25.0 g, 194 mmol) was dissolved in EtOH (ethanol) (200 mL). The solution was cooled to 0° C. and HCl gas bubbled through the solution for 30 minutes. The solution was stirred at ambient temperature for 16 h and then concentrated under vacuum. The residue was dissolved in EtOH (100 mL), cooled to 0° C. and a solution of NH3/MeOH (7M, 69 mL, 484 mmol) was added dropwise through an addition funnel. Once added, the solution was allowed to warm to ambient temperature and the resulting NH4Cl was filtered off. The solution was concentrated under vacuum and the resulting white solid was used without further purification (26 g crude).
後処理
- customHCl gas bubbled through the solution for 30 minutes
- concentrationconcentrated under vacuum
- dissolutionThe residue was dissolved in EtOH (100 mL)
- temperaturecooled to 0° C.
- additionOnce added
- temperatureto warm to ambient temperature
- filtrationthe resulting NH4Cl was filtered off
- concentrationThe solution was concentrated under vacuum
- customthe resulting white solid was used without further purification (26 g crude)
出典と根拠
- ORDレコード
- ord-32928aa9dc1446bfab1a8ab258d9abbc
- 出典データセット
- uspto-grants-2010_05
- 特許番号
- US07709483B2
関連ノート
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