反応式
C1([Si](OC)(OC)OC)C=CC=CC=1.C(O[Si](OCC)(OCC)OCC)C.C[Si](OCC)(OCC)OCC.[C:38]([O-:41])(=[O:40])[CH3:39].C(O[Si](CCC[NH+:55]1[CH2:59][CH2:58][N:57]=[CH:56]1)(OCC)OCC)C.Cl.C(OCC(O)C)C>O.CC(C)=O.CO.C(O)C>[C:38]([O-:41])(=[O:40])[CH3:39].[NH+:55]1[CH:59]=[CH:58][NH:57][CH:56]=1参加物
実験手順
4.92 g of phenyltrimethoxysilane, 72.46 g of tetraethoxysilane, 22.06 g of methyltriethoxysilane, 0.55 g of the 30% ethanol solution of triethoxysilylpropyl-4,5-dihydroimidazolium acetate, and 150 g of acetone were charged into a 500 mL flask to be dissolved and the resultant mixed solution was warmed while stirring the mixed solution with a magnetic stirrer to reflux. Next, 33.13 g of 0.01 M hydrochloric acid was added to the mixed solution. The mixed solution was subjected to the reaction for 240 minutes and then the resultant reaction solution was cooled down to room temperature. Then, 200 g of propylene glycol monoethyl ether was added to the reaction solution, and ethanol and methanol as reaction by-products, acetone, water, and hydrochloric acid were distilled off under reduced pressure to obtain a hydrolysis-condensation product. The polymer thus obtained corresponded to Formula (VII-8):
後処理
- dissolutionto be dissolved
- additionthe resultant mixed solution
- temperaturewas warmed
- temperatureto reflux
- customThe mixed solution was subjected to the reaction for 240 minutes
- customthe resultant reaction solution
- distillationwere distilled off under reduced pressure
- customto obtain a hydrolysis-condensation product
- customThe polymer thus obtained
出典と根拠
- ORDレコード
- ord-134d7bfa0b36436cbda5e086a15c433a
- 出典データセット
- uspto-grants-2014_10
- 特許番号
- US08864894B2
関連ノート
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