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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1085801Generated: October 26, 2026

1H-1,2,4-Triazole → 4-Chlorophenyl 2-(1,2,4-triazol-1-yl)-prop-2-yl ketone

https://huagongshe.com/reaction/1085801

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-1,2,4-TriazoleHCID 9257—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Bromo-1-(4-chlorophenyl)-2-methylpropan-1-oneHCID 11299973—
SolventAcetoneHCID 180—
Product4-Chlorophenyl 2-(1,2,4-triazol-1-yl)-prop-2-yl ketoneHCID 1336685525.7%

Reaction Steps

80 g (0.31 mole) of 2-bromo-prop-2-yl 4-chlorophenyl ketone, 26.9 g (0.39 mole) of 1,2,4-triazole and 53.8 g (0.39 mole) of potassium carbonate are heated under reflux in 350 ml of acetone for 6 hours. The mixture is allowed to cool and is filtered and the filtrate is concentrated in vacuo. The residue is taken up in methylene chloride and the mixture is washed with water, dried over sodium sulphate and concentrated in vacuo. The residue is recrystallised from diisopropyl ether. 19.9 g (25.7% of theory) of 4-chlorophenyl 2-(1,2,4-triazol-1-yl)-prop-2-yl ketone of melting point 111° C. are obtained. ##STR19##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05011850
Source datasetuspto-grants-1991_04
ORD IDord-277a6eaca078433b9231c2c716a58751
Source noteuspto-grants-1991_04