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1H-1,2,4-Triazole → Tebuconazole
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 | 2-tert-Butyl-2-(2-(4-chlorophenyl)ethyl)oxirane | HCID 94684 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | Tebuconazole | HCID 86102 | 53.3% |
反応手順
A solution of 17.9 g (0.075 mole) of 2-(4-chlorophenylethyl)-2-tert.-butyloxirane and 6.9 g (0.1 mole) of 1,2,4-triazole in 30 ml of ethanol in a sealed tube is heated at 150° C. for 20 hours. The tube is allowed to cool and the reaction solution is evaporated. The residue is dissolved in ether, washed three times with water and once with sodium chloride solution, dried over sodium sulphate and evaporated. The residue is chromatographed over a column of silican gel (mobile phase: dichloroethane/ethyl acetate 1:1). 12.3 g (53.2% of theory) of 1-(4-chlorophenyl)-4,4-dimethyl-3-(1,2,4-triazol-1-yl-methyl)-3-pentanol are obtained as a viscous oil.
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-7450237c8f7f43f99617dae5adba092e |
| 出典メモ | uspto-grants-1987_05 |