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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1401372Generated: October 30, 2026

Phenylacetylene → 4-(4-phenyl-1H-1,2,3-triazol-1-yl)pyridine

https://huagongshe.com/reaction/1401372

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylacetyleneHCID 10821—
Reactant4-AzidopyridineHCID 11332449—
ReactantSodium AscorbateHCID 23667548—
CatalystCopper SulfateHCID 24462—
SolventPropan-2-one--water (1/1)HCID 18366337—
Product4-(4-phenyl-1H-1,2,3-triazol-1-yl)pyridineHCID 102323493—

Reaction Steps

Approximately equimolar amounts of 4-azidopyridine and phenylacetylene (4.12 ml, 41.8 mmol) were added into a 250 mL round-bottom flask with 50 mL mixture of water/acetone. Copper (II) sulfate and sodium L-ascorbate were added to this solution and the reaction was stirred at room temperature for 24 hours. The solution was filtered and concentrated. Ethyl acetate (200 ml) was added to the concentrated solution. The organic layer was washed twice with 25 mL water, dried with MgSO4, filtered, concentrated and dried in vacuo, producing 4-(4-phenyl-1H-1,2,3-triazol-1-yl)pyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08907105B1
Source datasetuspto-grants-2014_12
ORD IDord-06f9e4861c7b43b489a1f59c84c5fbeb
Source noteuspto-grants-2014_12