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HRID 641094作成日:2026年10月26日

(+-)-Mercaptosuccinic acid → 2-Mercaptosuccinic acid bis-(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl) ester

https://huagongshe.com/reaction/641094

反応式

関与物質

役割名称HCID仕込み量
反応物(+-)-Mercaptosuccinic acidHCID 6268—
反応物3,3,4,4,5,5,6,6,7,7,8,8,8-Tridecafluorooctan-1-olHCID 69537—
触媒p-Toluenesulfonic acid monohydrateHCID 521998—
溶媒TolueneHCID 1140—
生成物2-Mercaptosuccinic acid bis-(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl) esterHCID 87503523100%

反応手順

Mercaptosuccinic acid (Aldrich) (12.5 g, 0.083 mole) and 1H,1H,2H,2H-perfluorooctan-1-ol (Fluorochem Ltd.) (60.6 g, 0.166 mole) were suspended in toluene (400 ml). p-Toluene sulfonic acid hydrate (Aldrich) (0.36 g) was added and the mixture refluxed under argon atmosphere for 72 hours in a flask equipped with a Dean & Stark reflux condenser. The solution was allowed to cool and the toluene was removed by evaporation under reduced pressure. The resulting oil was redissolved in ethyl acetate (1000 ml) and washed with saturated aqueous sodium hydrogen carbonate (800 ml). The organic layer was separated, dried over anhydrous magnesium sulfate, filtered and evaporated to give 2-mercaptosuccinic acid bis-(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl) ester as a pale yellow oil (66.2 g, 100% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07695783B2
出典データセットuspto-grants-2010_04
ORD IDord-b8918341361a48a6aaa1ef6b41966476
出典メモuspto-grants-2010_04