Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 557478Generated: October 25, 2026

p-Toluenesulfonic acid → Acrylic acid 3,3,4,4-tetrafluoro-4-heptafluoropropyloxy-butyl ester

https://huagongshe.com/reaction/557478

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantAcrylic AcidHCID 6581—
Reactant2-[2-(Heptafluoropropoxy)-tetrafluoroethyl]-ethyl alcoholHCID 57740575—
ProductAcrylic acid 3,3,4,4-tetrafluoro-4-heptafluoropropyloxy-butyl esterHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08058463B2
Source datasetuspto-grants-2011_11
ORD IDord-2ea0057a792c48289b1017ce5d390b31
Source noteuspto-grants-2011_11