化工社化工社 化学情報印刷レポート · 研究参考用
2-Bromo-2'-nitroacetophenone → 4-(2-Nitrophenyl)thiazole-2-amine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2-Bromo-2'-nitroacetophenone | HCID 244025 | — |
| 反応物 | Thiourea | HCID 2723790 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 4-(2-Nitrophenyl)thiazole-2-amine | HCID 595779 | — |
反応手順
4-(2-Nitro-phenyl)-thiazol-2-ylamine was prepared as follows: 2-Bromo-2′-nitroacetophenone (1.75 g, 7.2 mmol) was mixed with 50 mL of absolute EtOH along with thiourea (1.09 g, 14.4 mmol) and stirred under reflux for 2 hours. The reaction mixture was cooled to room temperature and concentrated under reduced pressure. The resulting residue was basified with 20 mL of 1 N aqueous NaOH and extracted with CH2Cl2. The combined organic layers were dried (Na2SO4) and concentrated to afford essentially quantitative yield of 4-(2-nitro-phenyl)-thiazol-2-ylamine.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08088928B2 |
| 出典データセット | uspto-grants-2012_01 |
| ORD ID | ord-f45d86eaa3234b0bbb13b75f84f29e24 |
| 出典メモ | uspto-grants-2012_01 |