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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 973674Generated: October 29, 2026

Propargyl bromide → HCID 20089150, compound

https://huagongshe.com/reaction/973674

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl bromideHCID 7842—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 67790043HCID 67790043—
SolventAcetoneHCID 180—
ProductHCID 20089150HCID 2008915069.2%

Reaction Steps

To the solution of 3-(4-chlorophenyl)-4-ethyl-1,2,4-triazolin-5-one (2.23 g, 0.01 mole) in dry acetone (40 ml) was added, at room temperature, potassium carbonate (1.67 g, 0.0012 mole) followed by propargyl bromide (1.8 g of 80% in toluene, 0.012 mole). The reaction mixture was then refluxed with stirring for 6 hr. The mixture was cooled down to room temperature and solvent was evaporated to give a residue. The product was purified by crystallization from hexane/ether, affording 1.8 g (69.2% yield) of 1-propargyl-3-(4-chlorophenyl)-4-ethyl-1,2,4-triazolin-5-one as a white solid, m.p. 115°-119° C. A proton NMR spectrum was consistent with the desired structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05064845
Source datasetuspto-grants-1991_11
ORD IDord-8cd6989ac75e45e5b465b70322621518
Source noteuspto-grants-1991_11