反応式
C(OCC#C)(=O)C=C.C[SiH](C)Cl.C(NCC)C.C(N([CH:23]=[CH:24][C:25]([O:27][CH2:28][CH:29]=[CH:30][Si:31]([CH3:34])([CH3:33])[Cl:32])=[O:26])CC)C.[SiH3]O>>[C:25]([O:27][CH2:28][CH:29]=[CH:30][Si:31]([CH3:34])([CH3:33])[Cl:32])(=[O:26])[CH:24]=[CH2:23]参加物
6
実験手順
Acryloxypropenyldimethylchlorosilane was prepared by a modification of Example 2 of U.S. Patent 3,746,734, to Berger et. al., using propargyl acrylate and dimethylchlorosilane as reactants. This product was then reacted with diethylamine. The resulting N,N-diethylaminoacryloxypropenyldimethylchlorosilane was then condensed with the 12000 MW and 28000 MW silanol terminated silicones utilized in Examples 1-16. The resulting acrylate terminated silicones were designated D and E, respectively.
後処理
- customterminated silicones
- customThe resulting acrylate terminated silicones
出典と根拠
- ORDレコード
- ord-85e7b92189dd4fb189d70890859470ec
- 出典データセット
- uspto-grants-1987_06
- 特許番号
- US04675346
関連ノート
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