Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 2,6-Xylyl isocyanate | HCID 98787 | — |
| Reactant | HCID 178508942 | HCID 178508942 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178424814 | HCID 178424814 | — |
Reaction Steps
A suspension of 6.95 g (0.0306 mole) of 5,5-diphenyl-2-amino-2-imidazoline-4-one in 300 ml of dry DMF is treated with 4.5 g (0.0306 mole) of 2,6-dimethylphenylisocyanate. The reaction mixture is stirred at 40°C for 2 hours. It is then poured into cold water and the resulting solids are filtered off. To the crude product is added 30 ml of water with heating; acetone is added to the heated slurry until all solids go in solution (1.5 liters of acetone). The solution is then evaporated to a volume of 300 ml., chilled, and the resulting solids are filtered off to give 1-(2,6-dimethylphenyl)-3-(5,5-diphenyl-4-oxo-2-imidazolidinylidene) urea, the pure product; no m.p. up to 350°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03983135 |
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| Source dataset | uspto-grants-1976_09 |
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| ORD ID | ord-aff76e9ce3d44ff3af596319d7e086b2 |
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| Source note | uspto-grants-1976_09 |
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