1,3-Dibromopropane → 1-Phenylcyclobutanecarbonitrile
反応式
[H-].[Na+].[C:3]1([CH2:9][C:10]#[N:11])[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.Br[CH2:13][CH2:14][CH2:15]Br.O.C1(C)C=CC=CC=1>CN(C=O)C>[C:3]1([C:9]2([C:10]#[N:11])[CH2:15][CH2:14][CH2:13]2)[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1参加物
6
反応条件
- 温度
- 0 °C
実験手順
Sodium hydride (1.54 g, 64.1 mmol) dissolved in DMF (15 ml) and cooled to 0° C. Phenyl acetonitrile (3 g, 25.6 mmol) and 1,3-dibromopropane (5.2 g, 25.6 mmol) were dissolved in DMF (15 ml) and added to above mixture drop-wise at 0° C. This mixture was heated to rt and continued stirring for 2 h. Work up (H2O/Toluene) afforded the title compound (2.61 g) as crude, which was used in the next without further purification.
後処理
- additionadded to above mixture drop-wise at 0° C
- temperatureThis mixture was heated to rt
出典と根拠
- ORDレコード
- ord-ab72727df51f4f6ca5969b20ac909818
- 出典データセット
- uspto-grants-2013_02
- 特許番号
- US08377970B2
反応ノート
読み込み中…