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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 25960Generated: October 29, 2026

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

https://huagongshe.com/reaction/25960

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-1,2,4-TriazoleHCID 9257—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Bromo-1,3-diphenylbutan-1-oneHCID 344863—
SolventMethyl Ethyl KetoneHCID 6569—
Product1,3-Diphenyl-2-(1H-1,2,4-triazol-1-yl)butan-1-oneHCID 21326061—

Reaction Steps

2-Bromo-3-phenyl-butyrophenone (0.02 mol), 1,2,4-triazole (0.02 mol) and potassium carbonate (0.04 mol) were refluxed in methyl ethyl ketone (100 ml) for 36 hours. After cooling to room temperature, the solution was filtered and the solvent removed in vacuo. Recrystallisation of the residue from ethanol/petroleum ether (60°-80°) gave the title compound as a colourless solid, m.p. 166°-8°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04147793
Source datasetuspto-grants-1979_04
ORD IDord-6d71dec87d5b41af88f4e662ee15c4e6
Source noteuspto-grants-1979_04