化工社化工社 化学情報印刷レポート · 研究参考用
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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | (+-)-Mercaptosuccinic acid | HCID 6268 | — |
| 反応物 | 3,3,4,4,5,5,6,6,7,7,8,8,8-Tridecafluorooctan-1-ol | HCID 69537 | — |
| 触媒 | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | 2-Mercaptosuccinic acid bis-(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl) ester | HCID 87503523 | 100% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US07695783B2 |
|---|
| 出典データセット | uspto-grants-2010_04 |
|---|
| ORD ID | ord-b8918341361a48a6aaa1ef6b41966476 |
|---|
| 出典メモ | uspto-grants-2010_04 |
|---|