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3-Chloro-4-hydroxy-5-methoxybenzaldehyde → 2-Cyano-3-(3-chloro-4-hydroxy-5-methoxyphenyl) propenanilide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 3-Chloro-4-hydroxy-5-methoxybenzaldehyde | HCID 29622 | — |
| 反応物 | Acetamide, 2-cyano-N-phenyl- | HCID 69296 | — |
| 触媒 | Piperidine | HCID 8082 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 2-Cyano-3-(3-chloro-4-hydroxy-5-methoxyphenyl) propenanilide | HCID 54181238 | 74.1% |
反応手順
To a solution of 5-chlorovanillin (728 mg, 3.9 mmol) and cyanoacetanilide (625 mg, 3.9 mmol) in ethanol (20 ml) were added 3 drops of piperidine, and the resulting mixture was refluxed for 2 hours. After cooling to room temperature, the resulting solid was filtered and washed with ethanol: water (1: 1) to give the objective 2-cyano-3-(3-chloro-4-hydroxy-5-methoxyphenyl) propenanilide (950 mg, 74% in yield).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05514711 |
| 出典データセット | uspto-grants-1996_05 |
| ORD ID | ord-ab545d1684904c21bbf62432b3ba8d21 |
| 出典メモ | uspto-grants-1996_05 |