Piperazine → 1-(But-3-yn-1-yl)piperazine
反応式
CC1C=CC(S(O[CH2:12][CH2:13][C:14]#[CH:15])(=O)=O)=CC=1.[NH:16]1[CH2:21][CH2:20][NH:19][CH2:18][CH2:17]1>CCO>[CH2:12]([N:16]1[CH2:21][CH2:20][NH:19][CH2:18][CH2:17]1)[CH2:13][C:14]#[CH:15]参加物
4
実験手順
A solution of but-3-ynyl 4-methylbenzenesulfonate (2.0 mL) and piperazine (2.0 g) in EtOH (6 mL) was heated to reflux for 30 min. The mixture was concentrated, diluted with NaOH 2 M (8 mL) and extracted with Et2O (50 mL). Evaporation of the organic layer gave a 2:1 mixture of mono and bis-alkylated piperazine (450 mg) which was discarded. The aqueous layer was further extracted with DCM (100 mL) to give of 1-(but-3-ynyl)piperazine (640 mg).
後処理
- temperatureto reflux for 30 min
- concentrationThe mixture was concentrated
- additiondiluted with NaOH 2 M (8 mL)
- extractionextracted with Et2O (50 mL)
- customEvaporation of the organic layer
- customgave
- extractionThe aqueous layer was further extracted with DCM (100 mL)
出典と根拠
- ORDレコード
- ord-8387ed94adb9408287ea3f9c30e02f6c
- 出典データセット
- uspto-grants-2012_01
- 特許番号
- US08093229B2
反応ノート
読み込み中…