HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Hydroxide → 1-(3-Methylphenyl)-5-phenyl-1H-1,2,4-triazole-3-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Potassium Bromide | HCID 253877 | — |
| Reactant | HCID 178425636 | HCID 178425636 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-(3-Methylphenyl)-5-phenyl-1H-1,2,4-triazole-3-carboxamide | HCID 13132136 | 63% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04492597 |
| Source dataset | uspto-grants-1985_01 |
| ORD ID | ord-5fec88f282a64ae5bf141b2f545a4cc0 |
| Source note | uspto-grants-1985_01 |