反応式
[NH:1]1[CH2:5][CH2:4][CH2:3][CH2:2]1.[CH3:6][C:7]1[CH:14]=[CH:13][CH:12]=[CH:11][C:8]=1[CH:9]=O.C([Cl:18])(=O)C>>[Cl-:18].[CH3:6][C:7]1[CH:14]=[CH:13][CH:12]=[CH:11][C:8]=1[CH:9]=[N+:1]1[CH2:5][CH2:4][CH2:3][CH2:2]1参加物
4
実験手順
The reaction of 8.2 ml (0.100 mol) pyrrolidine and 7.0 g (0.050 mol) 2-methylbenzaldehyde in accordance with general synthesis instructions 2 and subsequent reaction with 3.9 g (0.050 mol) acetyl chloride in accordance with general synthesis instructions 3 gave 6.6 g (corresponding to 63% of the yield calculated by theory) 1-(2-methyl-benzylidene)-pyrrolidinium chloride.
後処理
- customwith general synthesis instructions 3
出典と根拠
- ORDレコード
- ord-d745609141254580931317ff1b8db479
- 出典データセット
- uspto-grants-2006_08
- 特許番号
- US07091220B2
関連ノート
読み込み中…