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Potassium Iodide → Ethyl 2-(2-methyl-1H-indol-1-yl)acetate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Potassium Iodide | HCID 4875 | — |
| 反応物 | Bromoacetate | HCID 6226 | — |
| 反応物 | Acetonitrile | HCID 6342 | — |
| 反応物 | 2-Methylindole | HCID 7224 | — |
| 反応物 | Cesium carbonate | HCID 10796 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | Ethyl 2-(2-methyl-1H-indol-1-yl)acetate | HCID 28881253 | 82% |
反応手順
A solution of 2-methyl-1H-indole (1.0 g, 7.6 mmol) in acetonitrile (25 mL) was treated with 2-bromoacetate (2.54 mL, 22.9 mmol), cesium carbonate (2.10 g, 11.4 mmol) and potassium iodide (253 mg, 1.52 mmol) and the resulting mixture was stirred at room temperature for 16 h. The mixture was diluted with ethyl acetate, washed with water and brine, dried over sodium sulfate, filtered, and concentrated, and the residue was purified to give (2-methyl-indol-1-yl)-acetic acid ethyl ester (1.36 g, 82% yield). LCMS (m/z): 218.1 (M+1).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07943652B2 |
| 出典データセット | uspto-grants-2011_05 |
| ORD ID | ord-4a055437874c42678fffdf958803417e |
| 出典メモ | uspto-grants-2011_05 |