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Dimethylformamide → 10-Ethylphenothiazine-3-carbaldehyde
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Dimethylformamide | HCID 6228 | — |
| 反応物 | Potassium Hydroxide | HCID 14797 | — |
| 反応物 | Phosphorus oxychloride | HCID 24813 | — |
| 反応物 | N-Ethylphenothiazine | HCID 219178 | — |
| 生成物 | 10-Ethylphenothiazine-3-carbaldehyde | HCID 314330 | — |
反応手順
Phosphorus oxychloride (POCl3,3.7 ml, 0.04 mol) was added dropwise to 4.4 ml (0.06 mol) of dry dimethylformamide (DMF) at 0° C. under a nitrogen atmosphere. This solution was warmed up slowly to room temperature. Then, a solution of 5 g (0.02 mol) of 10-ethylphenothiazine in dry DMF was added dropwise. The reaction mixture was refluxed at 80° C. for 24 hours and poured into the ice water. This solution was neutralized with potassium hydroxide until the pH reached 6–8. The product was extracted with chloroform. The chloroform extract was dried with anhydrous sodium sulfate, filtered and distilled. The product was crystallized from methanol. The yield of 10-ethylphenothiazine-3-carbaldehyde (C15H13NOS, FW=255.34) was 65%.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07083884B2 |
| 出典データセット | uspto-grants-2006_08 |
| ORD ID | ord-aab5b1b567764967a3b9eb9b16000b36 |
| 出典メモ | uspto-grants-2006_08 |