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Ethanol → N-(4-cyanophenyl)-4-amino-3-nitropyridine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ethanol | HCID 702 | — |
| 反応物 | 4-Aminobenzonitrile | HCID 13396 | — |
| 反応物 | 4-Chloro-3-nitropyridine | HCID 2735781 | — |
| 生成物 | N-(4-cyanophenyl)-4-amino-3-nitropyridine | HCID 19791284 | — |
反応手順
According to the method of J. C. S. Perkin Trans. I, 1979, 135, p-cyanoaniline (6.894 g, 58.4 mmol) was added to a solution of 4-chloro-3-nitropyridine (9.26 g, 58.4 mmol) in ethanol (200 ml) and the mixture was stirred at room temperature for 18 hours. The resulting yellow suspension was poured into 500 ml of ice-cold dilute ammonia and filtered. The solid was treated with 150 ml of boiling ethanol, cooled in ice, and filtered to give N-(4-cyanophenyl)-4-amino-3-nitropyridine, 12.15 g, as a bright yellow powder, m.p. 210°-211° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05248681 |
| 出典データセット | uspto-grants-1993_09 |
| ORD ID | ord-2bc83680343e4dc3bafc2ceb0ba1db4f |
| 出典メモ | uspto-grants-1993_09 |