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HRID 330442作成日:2026年10月26日

1H-1,2,4-Triazole → Tebuconazole

https://huagongshe.com/reaction/330442

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.-butyl-oxirane and 6.9 g (0.1 mole) of 1,2,4-triazole in 30 ml of ethanol was heated in a bomb tube at 150° C. for 20 hours. The reaction solution was allowed to cool and was concentrated. The residue was dissolved in ether and the solution was washed three times with water and once with sodium chloride solution, dried over sodium sulphate and concentrated. The residue was chromatographed over a silica gel column (mobile phase: methylene chloride/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)-pentane-3-ol were obtained as a viscous oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04897107
出典データセットuspto-grants-1990_01
ORD IDord-af2bb915808c42a3af71ad047fac0d91
出典メモuspto-grants-1990_01