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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 568314Generated: October 30, 2026

1H-1,2,4-Triazole → 4-(4-Chlorophenyl)-3,3-dimethyl-1-(1H-1,2,4-triazol-1-yl)butan-2-one

https://huagongshe.com/reaction/568314

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-1,2,4-TriazoleHCID 9257—
ReactantPotassium CarbonateHCID 11430—
Reactant1-Bromo-4-(4-chlorophenyl)-3,3-dimethylbutan-2-oneHCID 13286525—
SolventAcetoneHCID 180—
Product4-(4-Chlorophenyl)-3,3-dimethyl-1-(1H-1,2,4-triazol-1-yl)butan-2-oneHCID 13286526356.2%

Reaction Steps

37 g (0.13 mol) of 4-bromo-1-(4-chlorophenyl)-2,2-dimethyl-3-butanone, 13.3 g (0.019 mol) of 1,2,4-triazole and 53.8 g (0.39 mol) of potassium carbonate are heated under reflux in 300 ml of acetone for 8 hours. The mixture is allowed to cool, the inorganic residue is filtered off with suction and the filtrate is concentrated. The residue is taken up in chloroform and the mixture is washed with water, dried over sodium sulphate and concentrated. The residue is stirred with diethyl ether, filtered off with suction and dried at 50° C. in vacuo. 18.8 g (52% of theory) of 1-(4-chlorophenyl)-2,2-dimethyl-4-(1,2,4-triazol-1-yl)-3-butanone of melting point 127° C. are obtained. ##STR18##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04728356
Source datasetuspto-grants-1988_03
ORD IDord-2c995d242f9b4e77827f94366a679aff
Source noteuspto-grants-1988_03