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1H-1,2,4-Triazole → 3,4-Dihydro-2-(1H-1,2,4-triazole-1-yl)1(2H)-Naphthalenone
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(2H)-Naphthalenone, 2-bromo-3,4-dihydro- | HCID 101120 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 3,4-Dihydro-2-(1H-1,2,4-triazole-1-yl)1(2H)-Naphthalenone | HCID 14698800 | — |
反応手順
To a mixture of 30 g. potassium carbonate, 15 g. 1,2,4-triazole and 250 ml acetonitrile at 40° C. was added a solution of 45 g. 3,4-dihydro-2-bromo-1(2H)-naphthalenone in 150 ml acetonitrile. The mixture was allowed to react for 5 hours at 40° C. and than at reflux temperature for 2 hours. The solid was removed by filtration and the filtrate concentrated to dryness leaving a solid residue. This was dissolved in dichloromethane and washed twice with water. The organic extract was dried over sodium sulfate and evaporated to give 42 grams of product having a melting point of 96°-98° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05211736 |
| 出典データセット | uspto-grants-1993_05 |
| ORD ID | ord-03d5c0cd105e4024bc952133e486760d |
| 出典メモ | uspto-grants-1993_05 |