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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1759034Generated: October 26, 2026

Nitric Acid → 3-methyl-4-phenyl-4H-1,2,4-triazole

https://huagongshe.com/reaction/1759034

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
ReactantPhenyl IsothiocyanateHCID 7673—
ReactantAcetohydrazideHCID 14039—
ReactantAmmonium HydroxideHCID 14923—
SolventEthanolHCID 702—
Product3-methyl-4-phenyl-4H-1,2,4-triazoleHCID 12216908—

Reaction Steps

2.5 mol of phenyl isothiocyanate (Formula XXI of Chart B) is added to 0.5 mol of acethydrazide (Formula IV of Chart B) in 500 ml of absolute ethanol and refluxed for one hour, cooled and filtered. This is then dissolved in a solution of 28.0 gm sodium hydroxide in 400 ml of water and the mixture is refluxed for two hours. The reaction mixture is cooled in an ice bath and treated with 100 ml of concentrated hydrochloric acid. The resulting solid is filtered and recrystallized. 66.7 mmol of the solid is added to 53 ml of 20% nitric acid and heated on a steam bath. When the vigorous exothermic reaction is complete, an additional 53 ml of 20% nitric acid is added, and an additional 66.7 mmol of previous solid. Portions of the solid are reacted with nitric acid until all of the previous solid is reacted. After the final addition the reaction mixture is heated twenty minutes on a steam bath, cooled to ambient temperature and poured into cold 15% aqueous ammonium hydroxide solution. The subtitled product is extracted with chloroform, dried and concentrated to yield 3-methyl-4-phenyl-4H-1,2,4-triazole, (Formula XXIV, Chart B) mp 109°-111° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04338453
Source datasetuspto-grants-1982_07
ORD IDord-ee4e0a37541a4d8489efcb2602a43d99
Source noteuspto-grants-1982_07