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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1966670Generated: October 26, 2026

1H-1,2,4-Triazole → 5-Methoxy-2-1,2,4-triazol-1-yl-benzaldehyde

https://huagongshe.com/reaction/1966670

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-1,2,4-TriazoleHCID 9257—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Fluoro-5-methoxybenzaldehydeHCID 2734872—
SolventDimethyl SulfoxideHCID 679—
Product5-Methoxy-2-1,2,4-triazol-1-yl-benzaldehydeHCID 5854189220.2%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 2-fluoro-5-methoxybenzaldehyde (200 mg, 1.29 mmol) in DMSO (10 mL) are added 1,2,4-triazole (134 mg, 1.95 mmol) and K2CO3 (359 mg, 2.60 mmol) at room temperature. The solution is heated to 100° C. for 2 hours. The solution is cooled and is extracted with H2O (30 mL) and EtOAc (3×15 mL). The combined organic layer is dried with MgSO4 and is filtered. The filtrate is concentrated and the residue is purified by silica gel flash column chromatography with 50% EtOAc in heptane as the eluent to afford 5-methoxy-2-1,2,4-triazol-1-yl-benzaldehyde (53 mg, 20%) as a white foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08420655B2
Source datasetuspto-grants-2013_04
ORD IDord-892d70ed77a44ebba42cd5daa18731c8
Source noteuspto-grants-2013_04