戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 979451作成日:2026年10月26日

1H-1,2,4-Triazole → Tebuconazole

https://huagongshe.com/reaction/979451

反応式

関与物質

役割名称HCID仕込み量
反応物1H-1,2,4-TriazoleHCID 9257—
反応物2-tert-Butyl-2-(2-(4-chlorophenyl)ethyl)oxiraneHCID 94684—
溶媒EthanolHCID 702—
生成物TebuconazoleHCID 8610253.3%

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US04668660
出典データセットuspto-grants-1987_05
ORD IDord-7450237c8f7f43f99617dae5adba092e
出典メモuspto-grants-1987_05