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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 502421Generated: October 26, 2026

1H-1,2,4-Triazole → 3,5-Diethoxy-4-[1,2,4]triazol-1-yl-benzaldehyde

https://huagongshe.com/reaction/502421

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-1,2,4-TriazoleHCID 9257—
ReactantPotassium CarbonateHCID 11430—
Reactant3,5-Diethoxy-4-fluoro-benzaldehydeHCID 59128273—
SolventDimethyl SulfoxideHCID 679—
Product3,5-Diethoxy-4-[1,2,4]triazol-1-yl-benzaldehydeHCID 5870633185.6%

Reaction Conditions

Temperature110 °C

Reaction Steps

5.00 g (23.6 mMol) of 3,5-diethoxy-4-fluoro-benzaldehyde (example 50 g), 3.25 g (=2.0 eq.) of 1,2,4-triazole and 6.51 g (=2.0 eq.) of potassium carbonate was dissolved under argon in 50 mL of DMSO; the reaction mixture was stirred for 1 hour at 110° C. Then, it was cooled down to ambient temperature, poured into crashed ice and extracted twice with ethyl acetate. The organic phases were washed with water, dried over MgSO4, filtered and evaporated i.V. The crude product was purified by chromatography (silicagel, eluent:gradient of n-heptane/ethyl acetate) to yield 5.28 g of the title compound as colorless solid. MS: 261.9 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07772253B2
Source datasetuspto-grants-2010_08
ORD IDord-0f25d7d5e1b64cccb9ce6e8aadd3468f
Source noteuspto-grants-2010_08