反応式
[N:1]1[C:9]2[CH2:8][CH2:7][CH2:6][C:5]=2[CH:4]=[CH:3][CH:2]=1.[CH:10](=O)[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1.C(OC(=O)C)(=O)C>>[CH:10](=[C:8]1[C:9]2[N:1]=[CH:2][CH:3]=[CH:4][C:5]=2[CH2:6][CH2:7]1)[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1参加物
4
実験手順
15 g (0.125 mol) of 6,7-dihydro-5H-[1]pyrindine, 20.1 g (0.19 mol) of freshly destilled benzaldehyde and 24.5 g (0.24 mol) of acetic acid anhydride were heated under reflux for 24 h. The reaction mixture was evaporated, the residual oil dissolved in methylene chloride, the solution extracted with 1N NaOH solution, and the organic phase dried and evaporated. The residue was destilled under reduced pressure to give 19.3 g (75%) of the title compound.
後処理
- temperatureunder reflux for 24 h
- customThe reaction mixture was evaporated
- dissolutionthe residual oil dissolved in methylene chloride
- extractionthe solution extracted with 1N NaOH solution
- customthe organic phase dried
- customevaporated
出典と根拠
- ORDレコード
- ord-b4246cd9d8eb40b4b6de6d466dbf1014
- 出典データセット
- uspto-grants-2006_09
- 特許番号
- US07105513B2
関連ノート
読み込み中…