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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 979451Generated: October 25, 2026

1H-1,2,4-Triazole → Tebuconazole

https://huagongshe.com/reaction/979451

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-1,2,4-TriazoleHCID 9257—
Reactant2-tert-Butyl-2-(2-(4-chlorophenyl)ethyl)oxiraneHCID 94684—
SolventEthanolHCID 702—
ProductTebuconazoleHCID 8610253.3%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04668660
Source datasetuspto-grants-1987_05
ORD IDord-7450237c8f7f43f99617dae5adba092e
Source noteuspto-grants-1987_05