反応式
[CH2:1](Cl)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH3:16].[C:18]([NH2:22])(=[O:21])[CH:19]=[CH2:20].[Cl-].[Al+3].[Cl-].[Cl-].Cl>O.CC(C)=O>[CH2:1]([NH:22][C:18](=[O:21])[CH:19]=[CH2:20])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH3:16]参加物
7
実験手順
In a 250 ml capacity conical flask 13 g cetyl chloride (0.05 M), 3.5 g acrylamide (0.05 M) and 50 ml acetone were placed to obtain a clear solution. The solution was stirred with a magnetic needle at room temperature. 6.5 g anhydrous aluminium chloride (0.05 M) was added and the reaction mixture was stirred at room temperature. After 5 to 10 minutes of stirring, vigorous evolution of hydrogen chloride took place which ceased after about 5 minutes. Temperature of the reaction mixture was raised to 40 to 50° C. It was then cooled to room temperature and poured into 500 ml cold water. White product was precipitated. The product was isolated and purified by reprecipitation from acetone into cold water.
後処理
- customto obtain a clear solution
- stirringthe reaction mixture was stirred at room temperature
- stirringAfter 5 to 10 minutes of stirring
- temperatureTemperature of the reaction mixture was raised to 40 to 50° C
- temperatureIt was then cooled to room temperature
- customWhite product was precipitated
- customThe product was isolated
- custompurified by reprecipitation from acetone into cold water
出典と根拠
- ORDレコード
- ord-eaf1af5461a34344a0ac78c0f3a7fbe9
- 出典データセット
- uspto-grants-2002_04
- 特許番号
- US06369249B1
関連ノート
読み込み中…