化工社化工社 化学情報印刷レポート · 研究参考用
P-Anisidine → 2-(4-(4-Methoxyphenylamino)-3-nitrophenyl)benzoxazole
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | P-Anisidine | HCID 7732 | — |
| 反応物 | Sodium Bicarbonate | HCID 516892 | — |
| 反応物 | 2-(4-Fluoro-3-nitrophenyl)benzoxazole | HCID 21990970 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 2-(4-(4-Methoxyphenylamino)-3-nitrophenyl)benzoxazole | HCID 67498209 | 86% |
反応手順
To a suspension of 2-(4-fluoro-3-nitrophenyl)benzoxazole (see Working Example 15-2) (300 mg, 1.19 mmol) in ethanol (5 mL) was added sodium hydrogen carbonate (295 mg, 2.32 mmol) and p-anisidine (357 mg, 2.90 mmol), and this was heated to reflux with stirring for 4 hours. After the reaction was complete, this was cooled to room temperature, the precipitated crystals were filtered off, and after washing with water and ethanol the crystals were dried to yield the title compound (359 mg, 86% yield) as orange crystals.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08829035B2 |
| 出典データセット | uspto-grants-2014_09 |
| ORD ID | ord-971270a2eab341f2963d927eae88f57b |
| 出典メモ | uspto-grants-2014_09 |