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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1249148Generated: October 31, 2026

1H-1,2,4-Triazole → 1-(4-Chlorophenoxy)-3-methyl-1-(1,2,4-triazol-1-yl)-3-trifluoromethylthio-butan-2-one

https://huagongshe.com/reaction/1249148

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-1,2,4-TriazoleHCID 9257—
Reactant1-Bromo-1-(4-chlorophenoxy)-3-methyl-3-trifluoromethylthio-butan-2-oneHCID 13117303—
SolventAcetonitrileHCID 6342—
Product1-(4-Chlorophenoxy)-3-methyl-1-(1,2,4-triazol-1-yl)-3-trifluoromethylthio-butan-2-oneHCID 1311730437%

Reaction Steps

29 g (0.075 mol) of crude 1-bromo-1-(4-chlorophenoxy)-3-methyl-3-trifluoromethylthio-butan-2-one and 16 g (0.25 mol) of 1,2,4-triazole in 150 ml of acetonitrile were heated under reflux for 1 hour. Thereafter, the mixture was concentrated and the residue was taken up with methylene chloride/water. The organic phase was separated off, dried over sodium sulphate and concentrated again. The oil residue was chromatographed. 10.4 g (37% of theory) of 1-(4-chlorophenoxy)-3-methyl-1-(1,2,4-triazol-1-yl)-3-trifluoromethylthio-butan-2-one of melting point 66° C. were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04629732
Source datasetuspto-grants-1986_12
ORD IDord-258c49ee33d84da5a7ed1c23a456dcdb
Source noteuspto-grants-1986_12