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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1253127Generated: November 2, 2026

1H-1,2,4-Triazole → 3,3,4-Trimethyl-1-(1H-1,2,4-triazol-1-yl)pentan-2-one

https://huagongshe.com/reaction/1253127

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-1,2,4-TriazoleHCID 9257—
ReactantPotassium CarbonateHCID 11430—
Reactant1-Chloro-3,3,4-trimethylpentan-2-oneHCID 13295226—
SolventEthanolHCID 702—
Product3,3,4-Trimethyl-1-(1H-1,2,4-triazol-1-yl)pentan-2-oneHCID 1329522779.3%

Reaction Conditions

Temperature40 °C

Reaction Steps

162.5 g (1 mol) of 1-chloro-3,3,4-trimethylpentan-2-one are added dropwise to a suspension of 84 g (1.2 mols) of 1,2,4-triazole and 165.6 g (1.2 mols) of potassium carbonate in 1 liter of ethanol. The mixture is stirred for 15 hours at 40° C., the inorganic precipitate is filtered off under suction, the solvent is distilled off, the precipitate is taken up in 500 ml of methylene chloride, the organic phase is extracted with 1 liter of water, the aqueous phase is extracted with 500 ml of methylene chloride, the methylene chloride phases are combined, and the combined phases are extracted with twice 1 liter of water. The solvent is distilled off from the organic phase. 154.6 g (79.3% of theory) of 1-(1,2,4-triazol-1-yl)-3,3,4-trimethylpentan-2-one are obtained as a colorless oil of refractive index nD20 =1.4827. ##STR16##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04747869
Source datasetuspto-grants-1988_05
ORD IDord-19dde3c20ea545b2aa8ff9e78b990536
Source noteuspto-grants-1988_05