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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1608250Generated: November 1, 2026

1H-1,2,4-Triazole → Tebuconazole

https://huagongshe.com/reaction/1608250

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-chlorophenyl-ethyl)-2-tert.-butyl-oxirane and 6.9 g (0.1 mole) of 1,2,4-triazole in 30 ml of ethanol were heated at 150° C. in a bomb tube for 20 hours. The reaction mixture was allowed to cool and was concentrated. The residue was dissolved in ether and the ether 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)-pentan-3-ol were obtained as a viscous oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04870093
Source datasetuspto-grants-1989_09
ORD IDord-fc436b76ba6d4b6097827723baf21ced
Source noteuspto-grants-1989_09