反応式
[CH2:1]([O:4][CH2:5][CH:6]1[O:8][CH2:7]1)[CH:2]=[CH2:3].[CH2:9]([SiH:12]([O:15][CH3:16])[O:13][CH3:14])[CH:10]=[CH2:11]>C(O)(C)C.[H+].[H+].Cl[Pt-2](Cl)(Cl)(Cl)(Cl)Cl>[CH3:14][O:13][Si:12]([O:15][CH3:16])([CH2:3][CH2:2][CH2:1][O:4][CH2:5][CH:6]1[O:8][CH2:7]1)[CH2:9][CH:10]=[CH2:11]参加物
5
実験手順
Using the same apparatus and procedure described in EXAMPLE 1, 12.1 g (0.11 mmol) of allylglycidyl ether and 60 μl of 1% chloroplatinic acid in isopropanol were added to the flask. Through the dropping funnel was added dropwise 6.6 g (0.05 mmol) of allyldimethoxysilane at 80° C. and the solution was further reacted for 2 hrs to complete the reaction. Vacuum distillation (83°-85° C.) of the product mixture gave 5.3 g (43.5%) of 4,4-dimethoxy-7-glycidoxy-4-sila-1-heptene.
後処理
- additionwere added to the flask
- customthe solution was further reacted for 2 hrs
- customthe reaction
- distillationVacuum distillation (83°-85° C.) of the product mixture
出典と根拠
- ORDレコード
- ord-e291784d8c894ca985aa7ae4f96346ae
- 出典データセット
- uspto-grants-1995_05
- 特許番号
- US05420323
関連ノート
読み込み中…