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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1488492Generated: November 4, 2026

Sodium Iodide → HCID 10830980, compound

https://huagongshe.com/reaction/1488492

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
Reactant4-Nitrobenzyl bromideHCID 66011—
Reactant4-Nitrophenyl(1,2,4-triazol-4-yl)amineHCID 10845888—
SolventMethyl Ethyl KetoneHCID 6569—
ProductHCID 10830980HCID 1083098045.6%

Reaction Steps

To a suspension of 0.37 g of 4-[(4-nitrophenyl)amino]-4H-1,2,4-triazole obtained in Referential Example 3 in 20 ml of 2-butanone were successively added 0.83 g of potassium carbonate anhydride, 1.30 g of p-nitrobenzyl bromide and a catalytic amount of sodium iodide, at room temperature, and the reaction mixture was then heated under reflux for about 2 hours. After cooled, the solvent was removed by distillation under reduced pressure, and a proper amount of water was added to the residue, which was then extracted several times each with ethyl acetate. The ethyl acetate layer separated was washed with water and dried over anhydrous magnesium sulfate, and the solvent was removed by distillation under reduced pressure. The residue formed was purified by silica gel column chromatography to give crude crystals from the chloroform/methanol (100/1) eluate. The crude crystals thus obtained were recrystallized from ethanol to give 0.28 g of 4-[N-(4-nitrobenzyl)-N-(4-nitrophenyl)amino]-4H-1,2,4-triazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05674886
Source datasetuspto-grants-1997_10
ORD IDord-35b8c72f4cb64491a0069754aec54fe5
Source noteuspto-grants-1997_10