Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
p-Toluenesulfonic acid → Acrylic acid 3,3,4,4-tetrafluoro-4-heptafluoropropyloxy-butyl ester
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | p-Toluenesulfonic acid | HCID 6101 | — |
| 반응물 | Acrylic Acid | HCID 6581 | — |
| 반응물 | 2-[2-(Heptafluoropropoxy)-tetrafluoroethyl]-ethyl alcohol | HCID 57740575 | — |
| 생성물 | Acrylic acid 3,3,4,4-tetrafluoro-4-heptafluoropropyloxy-butyl ester | HCID 86631012 | — |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08058463B2 |
| 출처 데이터셋 | uspto-grants-2011_11 |
| ORD ID | ord-2ea0057a792c48289b1017ce5d390b31 |
| 출처 메모 | uspto-grants-2011_11 |