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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 330442Generated: October 25, 2026

1H-1,2,4-Triazole → Tebuconazole

https://huagongshe.com/reaction/330442

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.-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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04897107
Source datasetuspto-grants-1990_01
ORD IDord-af2bb915808c42a3af71ad047fac0d91
Source noteuspto-grants-1990_01