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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2248605Generated: October 31, 2026

4-Fluorobenzaldehyde → N-[(4-Fluorophenyl)methylene]-1H-1,2,4-triazol-1-amine

https://huagongshe.com/reaction/2248605

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-FluorobenzaldehydeHCID 68023—
Reactant1H-1,2,4-triazol-1-amineHCID 11708047—
Catalystp-Toluenesulfonic acidHCID 6101—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductN-[(4-Fluorophenyl)methylene]-1H-1,2,4-triazol-1-amineHCID 5427101668.3%

Reaction Steps

A solution of 42.3 g (0.377 mol) of 75% pure 1-amino-1H-1,2,4-triazole, 40.0 mL (0.372 mol) of 4-fluorobenzaldehyde and 2.0 g of p-toluenesulfonic acid in 600 mL of tetrahydrofuran was stirred at room temperature for 21/2 days. The reaction mixture was diluted with ethyl acetate, washed with saturated aqueous Na2CO3, water and brine and dried (MgSO4). Removal of solvent gave a white solid which was recrystallized from n-butylchloride to afford 48.3 g (67%) of desired product as white needles; mp 118°-120° C. Concentration of the filtrate and recrystallization of the residue afforded 12.8 g (18%) more of product; mp 118°-120° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05041458
Source datasetuspto-grants-1991_08
ORD IDord-11be9ab357cd4cbd8e6f3ccf371198fa
Source noteuspto-grants-1991_08