Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Aniline | HCID 6115 | — |
| Reactant | Phenyl isocyanate | HCID 7672 | — |
| Reactant | Dabco | HCID 9237 | — |
| Reactant | Hydantoin | HCID 10006 | — |
| Reactant | N-Phenylmaleimide | HCID 13662 | — |
| Solvent | 1,2-Dichlorobenzene | HCID 7239 | — |
| Product | HCID 54452345 | HCID 54452345 | — |
Reaction Steps
26.6 parts of the compound ##STR5## (from aniline and N-phenyl maleic imide) are dissolved in 100 ml of o-dichlorobenzene. 11.9 parts of phenylisocyanate are added and the reaction mixture is left to stand overnight. After the addition of 0.1 g of 1,4-diaza-bicyclo-[2,2,2]-octane, the solution is stirred for 6 hours at 175° C., the solvent is distilled off under vacuum and toluene is added to the residue. The crystalline precipitate obtained is suction filtered and recrystallised from ethyl acetate. The structure obtained by calculation is confirmed by the NMR- and IR-spectra (for hydantoin 1715 and 1770 cm-1 ; for amide 1690 cm-1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04170701 |
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| Source dataset | uspto-grants-1979_10 |
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| ORD ID | ord-e5e0af98372b4a34ac73984ae3dbad52 |
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| Source note | uspto-grants-1979_10 |
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