HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,6-Xylyl isocyanate → N-(1,3-Dimethyl-4-oxoimidazolidin-2-ylidene)-N'-(2,6-dimethylphenyl)urea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,6-Xylyl isocyanate | HCID 98787 | — |
| Reactant | 2-Imino-1,3-dimethylimidazolidin-4-one | HCID 14060427 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(1,3-Dimethyl-4-oxoimidazolidin-2-ylidene)-N'-(2,6-dimethylphenyl)urea | HCID 54230876 | — |
Reaction Steps
A mixture of 6.35 g (0.050 mole) of 1,3-dimethyl-2-iminoimidazolidin-4-one and 7.25 g (0.050 mole) of 2,6-dimethylphenylisocyanate in 75 ml. of dry tetrahydrofuran is stirred at room temperature for two hours followed by refluxing it for thirty minutes. The reaction mixture is evaporated in vacuo to give a solid, which is crystallized from tetrahydrofuran-ether. Two more recrystallizations from the same solvent mixture gives pure product, 1-(1,3-dimethyl-4-oxo-2-imidazolidinylidene)-3-(2,6-dimethylphenyl) urea; m.p. 115.5°-118.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04025517 |
| Source dataset | uspto-grants-1977_05 |
| ORD ID | ord-b7ac7b709ef247918f3412a03121a2a4 |
| Source note | uspto-grants-1977_05 |