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Formaldehyde → 4-(5-Methoxy-1,3,4-thiadiazol-2-yl)-2-propyl-1,2,4-triazolidin-3-one
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Formaldehyde | HCID 712 | — |
| 反応物 | Potassium Hydroxide | HCID 14797 | — |
| 反応物 | N-(5-Methoxy-1,3,4-thiadiazol-2-yl)-1-propylhydrazine-1-carboxamide | HCID 21454627 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 4-(5-Methoxy-1,3,4-thiadiazol-2-yl)-2-propyl-1,2,4-triazolidin-3-one | HCID 21454646 | — |
反応手順
2-Propyl-4-(5-methoxy-1,3,4-thiadiazol-2-yl)-semicarbazide (0.1 mole) dissolved in methanol (100 ml) is charged into a glass reaction vessel equipped with a mechanical stirrer and thermometer. Aqueous formaldehyde (0.2 mole; 37% concentration) is then added to the reaction vessel with stirring. Dilute aqueous potassium hydroxide is added to the reaction mixture to adjust the pH to between 7 and 8 and stirring is continued for a period of about 20 minutes resulting in the formation of a solid precipitate. The precipitate is recovered by filtration, is recrystallized and is dried under vacuum to yield the desired product 2-propyl-4-(5-methoxy-1,3,4-thiadiazol-2-yl)-1,2,4-triazolidin-3-one.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04007031 |
| 出典データセット | uspto-grants-1977_02 |
| ORD ID | ord-bb350c565cd54f499b21be07950a3cc5 |
| 出典メモ | uspto-grants-1977_02 |