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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1077605Generated: November 2, 2026

Acetic Acid → 3-Methyl-1-phenyl-4,5-dihydro-1H-1,2,4-triazol-5-one

https://huagongshe.com/reaction/1077605

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantPhenylhydrazineHCID 7516—
ReactantSodium CyanateHCID 517096—
ReactantN-phenyl-N'-(1-methoxyethylidene)hydrazineHCID 54154372—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product3-Methyl-1-phenyl-4,5-dihydro-1H-1,2,4-triazol-5-oneHCID 135537621—

Reaction Steps

A stirred solution of 2.0 grams (0.019 mole) of phenylhydrazine and 2.7 grams (0.022 mole-1.2 eq.) of TMOA in 20 mL of methanol is heated at reflux for about 1.5 hours, until the reaction to the intermediate N--phenyl--N'--(1-methoxyethylidene)hydrazine is complete. The progress of the reaction is monitored by gas chromatography (GC). After this time, the reaction mixture is cooled in an ice-water bath (0° C.) and 1.5 grams (0.022 mole-1.2 eq.) of sodium cyanate is added. Upon completion of addition, 1.3 grams (0.022 mole-1.2 eq.) of acetic acid is added dropwise. The reaction mixture is then stirred at the ice-water bath temperature for about 10 minutes, then it is allowed to warm to ambient temperature. After this time, two mL of water is added to the reaction mixture. Upon completion of addition, the reaction mixture is stirred at ambient temperature for about ten hours. The reaction mixture is concentrated under reduced pressure, yielding 4,5-dihydro-3-methyl-1-phenyl-1,2,4-triazol-5(1 H)-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05543541
Source datasetuspto-grants-1996_08
ORD IDord-e6b4f2dc78e3465cacbe681c5c1e4cfe
Source noteuspto-grants-1996_08