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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 989161Generated: October 29, 2026

N-vinyl-2-pyrrolidone → 1-Phenyl-1H-1,2,3-triazole

https://huagongshe.com/reaction/989161

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-vinyl-2-pyrrolidoneHCID 6917—
ReactantAzidobenzeneHCID 69319—
SolventEthanolHCID 702—
Product1-Phenyl-1H-1,2,3-triazoleHCID 270009—

Reaction Steps

In the method of preparation, the reaction between the N-vinylpyrrolidinone and the phenyl azide is carried out at room temperature in ethanol as solvent, and allowed to stand in the dark for several weeks, depending on the reactivity of the phenyl azides. Refluxing the reaction mixture eliminates the 5-(2-oxo-1-pyrrolidino) group and yields the 1-phenyl triazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06638954B2
Source datasetuspto-grants-2003_10
ORD IDord-2822d6e2988e481b8fd1cca2403860b8
Source noteuspto-grants-2003_10