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Water → 2-(5-Oxiranyl-furan-2-yl)-[1,3]dioxolane
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | Potassium Hydroxide | HCID 14797 | — |
| 反応物 | Sulfonium, trimethyl-, bromide (1:1) | HCID 2735154 | — |
| 反応物 | 5-(1,3-Dioxolan-2-yl)furan-2-carbaldehyde | HCID 14616597 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | 2-(5-Oxiranyl-furan-2-yl)-[1,3]dioxolane | HCID 23130765 | 102.1% |
反応手順
5-[1,3]Dioxolan-2-yl-furan-2-carbaldehyde (2.03 g, 12.1 mmol), trimethylsulfonium bromide (1.90 g, 12.1 mmol) and potassium hydroxide (779 mg, 13.9 mmol) were suspended in acetonitrile (75 mL), and the solution was stirred overnight at room temperature. Water was added to the reaction solution, which was then extracted with ethyl acetate, the organic layer was washed with brine and dried over anhydrous magnesium sulfate. The solvent was evaporated in vacuo, 2-(5-oxiranyl-furan-2-yl)-[1,3]dioxolane (2.25 g) was obtained as a pale yellow oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07932272B2 |
| 出典データセット | uspto-grants-2011_04 |
| ORD ID | ord-f386fb9bc7834aaca3b002b00c2987de |
| 出典メモ | uspto-grants-2011_04 |