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p-Toluenesulfonic acid → Acrylic acid 3,3,4,4-tetrafluoro-4-heptafluoropropyloxy-butyl ester
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | p-Toluenesulfonic acid | HCID 6101 | — |
| 反応物 | Acrylic Acid | HCID 6581 | — |
| 反応物 | 2-[2-(Heptafluoropropoxy)-tetrafluoroethyl]-ethyl alcohol | HCID 57740575 | — |
| 生成物 | Acrylic acid 3,3,4,4-tetrafluoro-4-heptafluoropropyloxy-butyl ester | HCID 86631012 | — |
反応手順
Acrylic acid was esterified with 2-[2-(heptafluoropropoxy)-tetrafluoroethyl]-ethyl alcohol (US 2008113199 A1) in the presence catalytic amounts of p-toluene sulfonic acid to yield acrylic acid 3,3,4,4-tetrafluoro-4-heptafluoropropyloxy-butyl ester quantitatively. The ester was washed with water and distilled prior to the reaction with APTES (Aminopropyl triethoxysilane, CAS#919-30-2). A solution of one equivalent of APTES and two equivalents acrylic acid 3,3,4,4-tetrafluoro-4-heptafluoropropyloxy-butyl in absolute ethanol were allowed to stir at 60° C. for 5 h. The solvent was distilled of under reduced pressure to provide the desired twin-tail silane (tertiary amine fluorosilane) quantitatively as a colorless oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08058463B2 |
| 出典データセット | uspto-grants-2011_11 |
| ORD ID | ord-2ea0057a792c48289b1017ce5d390b31 |
| 出典メモ | uspto-grants-2011_11 |