Dichlorodimethylsilane → 1-chloro-N-cyclohexyl-1,1-dimethylsilanamine
反応式
[Cl:1][Si:2](Cl)([CH3:4])[CH3:3].[CH:6]1([NH-:12])[CH2:11][CH2:10][CH2:9][CH2:8][CH2:7]1.[Li+].CCCCCC>C1COCC1>[Cl:1][Si:2]([CH3:4])([CH3:3])[NH:12][CH:6]1[CH2:11][CH2:10][CH2:9][CH2:8][CH2:7]1参加物
5
実験手順
In the drybox in a 250 mL flask 60.0 mL (490.89 mmol) of dichlorodimethylsilane was stirred in about 80 mL of THF. To this stirring solution 6.00 g (57.08 mmol) of lithium cyclohexylamide was added as a solid slowly and stirred overnight. The THF was removed under vacuum leaving a cloudy solution. Hexane was added to this mixture and the solids were filtered off and washed with hexane. The hexane was then removed from the filtrate under vacuum leaving a clear light yellow product weighing 9.18 g. Yield 84 percent.
後処理
- customThe THF was removed under vacuum
- customleaving a cloudy solution
- filtrationthe solids were filtered off
- washwashed with hexane
- customThe hexane was then removed from the filtrate under vacuum
- customleaving a clear light yellow product
出典と根拠
- ORDレコード
- ord-337fbac97c244d7aa63220a18b34e67a
- 出典データセット
- uspto-grants-2001_07
- 特許番号
- US06268444B1
反応ノート
読み込み中…