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1H-1,2,4-Triazole → 4-(1,2,4-Triazol-1-ylmethyl)benzonitrile
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 | 4-(Bromomethyl)benzonitrile | HCID 86996 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | 4-(1,2,4-Triazol-1-ylmethyl)benzonitrile | HCID 7537616 | — |
反応手順
A solution containing alpha-bromo-4-tolunitrile (19.6 g) and 1,2,4-triazole (30.5 g) in a mixture of chloroform (250 mL) and acetonitrile (50 mL) is stirred at reflux for 15 hours. The solution is cooled and washed with 3% aqueous sodium bicarbonate (200 mL) and the organic solution is then dried (MgSO4) and evaporated. The residue is chromatographed on silica gel (300 g). Elution with chloroform/isopropanol (10:1) affords 4-[1-(1,2,4-triazolyl)methyl]-benzontrile, m.p. 77°-79°, which forms a hydrochloride salt, m.p. 200°-205°, when its solution in ethyl acetate is treated with ethereal HCl.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04978672 |
| 出典データセット | uspto-grants-1990_12 |
| ORD ID | ord-75608f9dafaa46ef8d42a7355ab039bb |
| 出典メモ | uspto-grants-1990_12 |