Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 426649Generated: October 30, 2026

Aniline → HCID 54452345, compound

https://huagongshe.com/reaction/426649

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantPhenyl isocyanateHCID 7672—
ReactantDabcoHCID 9237—
ReactantHydantoinHCID 10006—
ReactantN-PhenylmaleimideHCID 13662—
Solvent1,2-DichlorobenzeneHCID 7239—
ProductHCID 54452345HCID 54452345—

Reaction Conditions

Temperature175 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04170701
Source datasetuspto-grants-1979_10
ORD IDord-e5e0af98372b4a34ac73984ae3dbad52
Source noteuspto-grants-1979_10