HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → Acrylic acid 3,3,4,4-tetrafluoro-4-heptafluoropropyloxy-butyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Acrylic Acid | HCID 6581 | — |
| Reactant | 2-[2-(Heptafluoropropoxy)-tetrafluoroethyl]-ethyl alcohol | HCID 57740575 | — |
| Product | Acrylic acid 3,3,4,4-tetrafluoro-4-heptafluoropropyloxy-butyl ester | HCID 86631012 | — |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08420826B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-279d0d6f894a46c6a4a5bdb8ab0ac941 |
| Source note | uspto-grants-2013_04 |