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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 979451생성일: 2026년 10월 24일

1H-1,2,4-Triazole → Tebuconazole

https://huagongshe.com/ko/reaction/979451

반응식

참여 물질

역할이름HCID투입량
반응물1H-1,2,4-TriazoleHCID 9257—
반응물2-tert-Butyl-2-(2-(4-chlorophenyl)ethyl)oxiraneHCID 94684—
용매EthanolHCID 702—
생성물TebuconazoleHCID 8610253.3%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04668660
출처 데이터셋uspto-grants-1987_05
ORD IDord-7450237c8f7f43f99617dae5adba092e
출처 메모uspto-grants-1987_05