Diethylamine → 2-Propenoic acid, 3-(chlorodimethylsilyl)-2-propen-1-yl ester

HRID 653138

反応式

HRID 653138 の反応式
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

  1. customterminated silicones
  2. 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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