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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1941344Generated: November 1, 2026

1H-1,2,4-Triazole → 4-(1H-1,2,4-triazol-1-yl)benzaldehyde

https://huagongshe.com/reaction/1941344

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-1,2,4-TriazoleHCID 9257—
ReactantPotassium CarbonateHCID 11430—
Reactant4-FluorobenzaldehydeHCID 68023—
CatalystHCID 178419072HCID 178419072—
SolventPyridineHCID 1049—
Product4-(1H-1,2,4-triazol-1-yl)benzaldehydeHCID 2776488—

Reaction Steps

A mixture of 1,2,4-triazole (4.06 g, 58.7 mmol), potassium carbonate (9.05 g, 65.5 mmol), 4-fluorobenzaldehyde (6.3 ml, 58.7 mmol), and copper(I) oxide (0.26 g, 1.82 mmol) in pyridine (30 ml) is heated under nitrogen atmosphere at reflux overnight. After pyridine is distilled, the residue is diluted with chloroform, filtered, and washed with chloroform. The combined filtrate is washed with water, dried over magnesium sulfate, and concentrated in vacuo. The crude material is purified by column chromatography on silica with hexane/ethyl acetate (1:2) to give 4-(1,2,4-triazol-1-yl)-benzaldehyde and with ethyl acetate/methanol (19:1) to give 4-(1,3,4-triazol-1-yl)-benzaldehyde.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05703106
Source datasetuspto-grants-1997_12
ORD IDord-98f2a17d58444bc39103f80ee88276d3
Source noteuspto-grants-1997_12