化工社化工社 化学情報印刷レポート · 研究参考用
Methyl iodide → 1H-Indole, 2,3-dihydro-1-methyl-5-nitro-
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Methyl iodide | HCID 6328 | — |
| 反応物 | Potassium Hydroxide | HCID 14797 | — |
| 反応物 | 5-Nitroindoline | HCID 36219 | — |
| 溶媒 | Acetone | HCID 180 | — |
| 生成物 | 1H-Indole, 2,3-dihydro-1-methyl-5-nitro- | HCID 167738 | 92% |
反応手順
To 5-nitroindoline (1.0 g, 6.1 mmol) in acetone (12 ml), powdered potassium hydroxide (1.7 g, 30.5 mmol, 5 eq) was added followed by the addition of methyl iodide (1.2 g, 9.1 mmol, 1.5 eq) at 0° C. The reaction mixture was stirred at room temperature overnight. The solvent was evaporated and water was added and the compound was extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate, filtered and concentrated to dryness to yield 1-methyl-5-nitro-2,3-dihydro-1H-indole (1.0 g, 92%). The crude compound was used in the next stage without purification.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08486962B2 |
| 出典データセット | uspto-grants-2013_07 |
| ORD ID | ord-dbef5ae2e9084970b97682d86da42dcd |
| 出典メモ | uspto-grants-2013_07 |