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Tetrahydrofuran → 4-Dodecanoxy-2-triethylsilylfuran
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Tetrahydrofuran | HCID 8028 | — |
| 反応物 | 1-Iodododecane | HCID 20282 | — |
| 反応物 | Potassium hydride | HCID 82127 | — |
| 反応物 | 4-Hydroxymethyl-2-triethylsilylfuran | HCID 15037035 | — |
| 生成物 | 4-Dodecanoxy-2-triethylsilylfuran | HCID 19019857 | — |
反応手順
A solution of 4-hydroxymethyl-2-triethylsilylfuran (Compound 1, 160 mg, 0.75 mmol) in tetrahydrofuran (0.5 ml) was added to a suspension of potassium hydride (33 mg, 0.83 mmol) in tetrahydrofuran (1 ml) at room temperature. When all the potassium hydride disappeared, 1-iodododecane (0.37 ml, 1.5 mmol) was added. Stirring was continued for 4 days at room temperature. The reaction mixture was quenched with water. Extraction (ethyl ether) and evaporation of the dried (magnesium sulfate) extracts gave an oil, which was purified by flash chromatography on silica using 5% ethyl ether/hexane. Fractions with Rf of about 0.65 on evaporation gave the titled ether as a pale yellow oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05298633 |
| 出典データセット | uspto-grants-1994_03 |
| ORD ID | ord-413aef5246c04bbdab4f6f30a2fe0bdb |
| 出典メモ | uspto-grants-1994_03 |