HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 1,2-Diphenyl-1,2,4-triazolidine-3,5-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Hydrazobenzene | HCID 31222 | — |
| Reactant | Ethyl N-(aminocarbonyl)carbamate | HCID 69380 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | 1,2-Diphenyl-1,2,4-triazolidine-3,5-dione | HCID 12565301 | — |
Reaction Steps
50 g (0.378 Mol) of ethylallophanate and 76.6 g (0.416 Mol) of 1,2-diphenylhydrazine were suspended in 100 ml of anhydrous xylene and refluxed for 6 hours with stirring, during which time ammonia was released. The solvent was distilled off, the residue was mixed with 150 ml of xylene once more and refluxed for 1 hour. The mixture was left to cool, the reaction product was suction filtered, and thoroughly washed with cold xylene. After drying in vacuo, 60.0 g (63% of theory) of colourless crystals were obtained, mp. 216°-217° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05807875 |
| Source dataset | uspto-grants-1998_09 |
| ORD ID | ord-40ec2afff7d74fcc8d31ee2ed8659371 |
| Source note | uspto-grants-1998_09 |