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1H-1,2,4-Triazole → 4-(2,4-Dichlorophenyl)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)butanone
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1H-1,2,4-Triazole | HCID 9257 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 1-Bromo-4-(2,4-dichlorophenyl)-3,3-dimethyl-2-butanone | HCID 13340381 | — |
| 溶媒 | Acetone | HCID 180 | — |
| 生成物 | 4-(2,4-Dichlorophenyl)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)butanone | HCID 13340382 | 45.6% |
反応手順
30 g (0.09 mole) of 1-bromo-4-(2,4-dichlorophenyl)-3,3-dimethyl-2-butanone, 12.4 g (0.18 mole) of 1,2,4-triazole and 24.8 g (0.18 mole) of potassium carbonate in 300 ml of acetone are heated under reflux for 6 hours. The mixture is then allowed to cool, the solid is filtered off with suction and the mother liquor is evaporated in vacuo. The residue is taken up in methylene chloride, and the solution is washed with water, dried over sodium sulphate and evaporated in vacuo. The residue is recrystallised from diethyl ether. 12.8 g (45.6% of theory) of 4-(2,4-dichlorophenyl)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)-2-butanone of melting point 85° C. are obtained.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04668660 |
| 出典データセット | uspto-grants-1987_05 |
| ORD ID | ord-b7de8dbd764244a89d31f25d6fa42932 |
| 出典メモ | uspto-grants-1987_05 |