化工社化工社 化学情報印刷レポート · 研究参考用
Imidazole → 3-(2-Iodoethyl)-7-methoxy-1-benzofuran
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Imidazole | HCID 795 | — |
| 反応物 | Iodine | HCID 807 | — |
| 反応物 | Triphenylphosphine | HCID 11776 | — |
| 反応物 | 3-(2-Hydroxyethyl)-7-methoxybenzofuran | HCID 22662935 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 3-(2-Iodoethyl)-7-methoxy-1-benzofuran | HCID 23614447 | — |
反応手順
To a stirred solution of 2-(7-methoxy-1-benzofuran-3-yl)ethanol (960 mg, 5 mmol) in anhydrous THF (50 ml), triphenylphosphine (1.572 g, 6 mmol), iodine (1.518 g, 6 mmol) and imidazole (408 mg, 6 mmol) were added at room temperature. The reaction mixture was stirred at room temperature for 4 hrs and quenched with water. The mixture was then extracted with chloroform, washed well with 5% Na2S2O3 solution and the organic layer dried over anhydrous MgSO4. It was then filtered and concentrated. The residue was purified by silica-gel column chromatography by eluting it with 30% ethyl acetate:hexane. The product, 2-(7-methoxy-1-benzofuran-3-yl)ethyl iodide, was obtained as a brown liquid. Yield: 1.3 g (86%); (M+H): 302.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07276603B2 |
| 出典データセット | uspto-grants-2007_10 |
| ORD ID | ord-f46e7d2007a84caf9d6ae20234802835 |
| 出典メモ | uspto-grants-2007_10 |