反応式
[CH2:1]=[CH:2][C:3]([CH3:6])([CH3:5])[CH3:4].[CH3:7][SiH:8]([Cl:10])[Cl:9].[SiH4]>C1COCC1.[H+].[H+].Cl[Pt-2](Cl)(Cl)(Cl)(Cl)Cl>[CH2:1]([Si:8]([CH3:7])([Cl:10])[Cl:9])[CH2:2][C:3]([CH3:6])([CH3:5])[CH3:4]参加物
6
反応条件
- 温度
- 42 °C
実験手順
A 2 liter, 4-necked flask equipped as in Example 1 was charged with 500 g (5.94 mol) of neohexene and 1 ml of a 10% chloroplatinic acid in THF solution. The mixture was heated to reflux (about 42° C.). 805 g (5.94 mol) of methyldichlorosilane was then added dropwise. After the addition of about 70 ml of the silane, the reaction commenced and the temperature in the flask rose to 102° C. as the remainder of the silane was added. The reaction mixture was allowed to cool to room temperature (about 25° C.) after the addition of the silane. Upon completion of the reaction, the remaining volatile components were removed at reduced pressure and the residue was distilled to give 1100 g (84% of theory) of neohexylmethyldichlorosilane.
後処理
- customA 2 liter, 4-necked flask equipped as in Example 1
- temperatureThe mixture was heated
- additionwas added
- temperatureto cool to room temperature (about 25° C.)
- customUpon completion of the reaction
- customthe remaining volatile components were removed at reduced pressure
- distillationthe residue was distilled
出典と根拠
- ORDレコード
- ord-61081ab86bd74aa48d58309b642acdf6
- 出典データセット
- uspto-grants-1994_03
- 特許番号
- US05296624
関連ノート
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