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HRID 557478作成日:2026年10月26日

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

https://huagongshe.com/reaction/557478

反応式

関与物質

役割名称HCID仕込み量
反応物p-Toluenesulfonic acidHCID 6101—
反応物Acrylic AcidHCID 6581—
反応物2-[2-(Heptafluoropropoxy)-tetrafluoroethyl]-ethyl alcoholHCID 57740575—
生成物Acrylic acid 3,3,4,4-tetrafluoro-4-heptafluoropropyloxy-butyl esterHCID 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

DOI10.6084/m9.figshare.5104873.v1
特許番号US08058463B2
出典データセットuspto-grants-2011_11
ORD IDord-2ea0057a792c48289b1017ce5d390b31
出典メモuspto-grants-2011_11