HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aniline → HCID 12876082, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aniline | HCID 6115 | — |
| Reactant | HCID 11062732 | HCID 11062732 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 12876082 | HCID 12876082 | 146.9% |
Reaction Steps
In 50 ml of anhydrous tetrahydrofuran, 7.4 g (0.08 mole) of aniline was dissolved. The mixture was cooled below 0° C., and a solution prepared by dissolving 6.4 g (0.04 mole) of 2,4,4-trimethylallophanoyl chloride in 10 ml of anhydrous tetrahydrofuran was added dropwise under stirring. The reaction was continued at a room temperature for 1 hour, then the solvent was removed by distillation under a reduced pressure, and water was added to form an insoluble matter. The insoluble matter was obtained by filtration and was recrystallized from ethanol to obtain 13.0 g (yield 73%) of 1,1,3-trimethyl-5-phenylbiuret having a melting point 89.5°-90.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04371544 |
| Source dataset | uspto-grants-1983_02 |
| ORD ID | ord-43bb54102b8745658bbd662d73efda79 |
| Source note | uspto-grants-1983_02 |