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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2412366Generated: October 29, 2026

Ammonium Hydroxide → 1-(3-Methylphenyl)-5-phenyl-1H-1,2,4-triazole-3-carboxamide

https://huagongshe.com/reaction/2412366

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
ReactantPotassium BromideHCID 253877—
ReactantHCID 178425636HCID 178425636—
SolventMethanolHCID 887—
Product1-(3-Methylphenyl)-5-phenyl-1H-1,2,4-triazole-3-carboxamideHCID 1313213663%

Reaction Steps

Three grams (0.01 mole) of 4-(3-methylphenyl-hydrazono)-2-phenyl-oxazoline-5-one (R1 =3--CH3, R2 =R3 =H in the formula II) was suspended in 93 ml of methanol. To the resulting suspension, 66.2 ml of 29% solution of ammonium hydroxide (0.549 mole) was added and refluxed for 5 minutes. Methanol and ammonia were then distilled off under a reduced pressure, and the resulting crystals were filtered out and washed with water. The crystals were recrystallized from a mixed solvent of 5.8 ml of methanol and 4.5 ml of water to obtain 1.8 g of almost colorless crystal, m.p. 142°-143° C., with a yield of 63%. I.R. (KBr, cm-1, refer to FIG. 2); 3500-3240 (broad and strong), 1700, 1670, 1610, 1458, 1400, 1302, 789 and 700.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04492597
Source datasetuspto-grants-1985_01
ORD IDord-5fec88f282a64ae5bf141b2f545a4cc0
Source noteuspto-grants-1985_01