反応式
[Cl-:1].[CH2:2]([P+](CCCC)(CCCC)CCCC)[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.[CH2:22](Cl)[C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1.[Cl:30][SiH2:31][Cl:32]>>[CH2:2]([SiH:31]([Cl:32])[Cl:30])[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.[CH2:22]([Si:31]([Cl:1])([Cl:32])[Cl:30])[C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1参加物
5
実験手順
In the same apparatus and procedure as Example 1 above, 0.26 g (0.79 mmol) of benyltributylphosphonium chloride, 1.01 ml (7.98 mmol) of benzyl chloride, and 2.42 g (24.0 mmol) of dichlorosilane were reacted at 150° C. for 2 hrs. The resulting mixture was distilled to give 0.29 g of benzyldichlorosilane (yield; 19%) and 0.95 g of benzyltrichlorosilane (yield; 53%).
後処理
- distillationThe resulting mixture was distilled
出典と根拠
- ORDレコード
- ord-380bfbcecc3d4ac1a46bb07f1b202964
- 出典データセット
- uspto-grants-2002_05
- 特許番号
- US06392077B1
関連ノート
読み込み中…