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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1488497Generated: November 4, 2026

Water → HCID 10774460, compound

https://huagongshe.com/reaction/1488497

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-Amino-1,2,4-triazoleHCID 11432—
Reactant5-Fluoro-2,1,3-benzoxadiazoleHCID 22905795—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 10774460HCID 1077446077.6%

Reaction Steps

26.70 Grams of potassium tert-butoxide was dissolved in 100 ml of anhydrous dimethylsulfoxide and 20.00 g of 4-amino-4H-1,2,4-triazole was added thereto, followed by stirring for 2 hours at room temperature. Next, 50 ml of an anhydrous dimethylsulfoxide solution containing 11.00 g of 5-fluorobenzofurazane was added dropwise to the solution over a period of 20 minutes and then the mixture was stirred for 15 minutes. The reaction mixture was poured into 500 ml of water and 500 g of ice and then washed with 200 ml of ethyl acetate. The solution was then adjusted to have pH of 7.0 with 1N hydrochloric acid to give crystals. The crystals were collected by filtration, and the remaining mother liquid was extracted with ethyl acetate. The organic layer was washed with water and a saturated aqueous sodium chloride solution and then dried over anhydrous sodium sulfate. The solvent was removed by distillation under reduced pressure, and the crude crystals thus obtained were recrystallized from ethanol. These were combined with the previously obtained crystals to give 12.49 g of 5-[(4H-1,2,4-triazol-4-yl)amino]benzofurazane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05674886
Source datasetuspto-grants-1997_10
ORD IDord-e0242654d16d40908f883a59605ac262
Source noteuspto-grants-1997_10