関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Tetraethoxysilane | HCID 6517 | — |
| 反応物 | 1-Ethoxy-2-propanol | HCID 15287 | — |
| 反応物 | Triethoxymethylsilane | HCID 16241 | — |
| 反応物 | Trimethoxyphenylsilane | HCID 18137 | — |
| 反応物 | HCID 67231912 | HCID 67231912 | — |
| 溶媒 | Acetone | HCID 180 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | HCID 67183781 | HCID 67183781 | — |
反応手順
4.92 g of phenyltrimethoxysilane, 72.40 g of tetraethoxysilane, 22.04 g of methyltriethoxysilane, 0.64 g of the 30% ethanol solution of triethoxysilylpropyl-4,5-dihydroimidazolium trifluoroacetate, 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, 33.10 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-9):
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08864894B2 |
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| 出典データセット | uspto-grants-2014_10 |
|---|
| ORD ID | ord-98971a6b61314a6097fed74287f9c92d |
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| 出典メモ | uspto-grants-2014_10 |
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