化工社化工社 化学情報印刷レポート · 研究参考用
Nitroethane → 6-fluoro-3-(2-nitropropenyl)-1H-indole
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Nitroethane | HCID 6587 | — |
| 反応物 | 6-Fluoroindole-3-carboxaldehyde | HCID 262903 | — |
| 反応物 | Ammonium Acetate | HCID 517165 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | 6-fluoro-3-(2-nitropropenyl)-1H-indole | HCID 66640512 | 86% |
反応手順
6-Fluoro-3-(2-nitropropenyl)-1H-indole was prepared by combining 6-fluoroindole-3-carboxaldehyde (485 mg, 2.97 mmol), nitroethane (6.0 mL), and ammonium acetate (250 mg, 3.27 mmol). The reaction solution was allowed to reflux 2 hours. The reaction solution was diluted with EtOAc (100 mL), washed with H2O (50 mL×2), partitioned, dried over Na2SO4, filtered, and concentrated under reduced pressure to provide 560 mg (86% yield) of 6-fluoro-3-(2-nitropropenyl)-1H-indole; 1H NMR (CDCl3) δ 11.03 (1H, br s), 8.41 (1H, s), 7.63 (1H, dd), 7.50 (1H, s), 7.06 (1H, dd), 6.92 (1H, t), 2.44 (3H, s); TLC (SiO2 plate, 100% DCM) Rf=0.7.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08524704B2 |
| 出典データセット | uspto-grants-2013_09 |
| ORD ID | ord-a6adde18e4e0446c863bbe24ebf188b1 |
| 出典メモ | uspto-grants-2013_09 |