87674-00-8Relevant academic research and scientific papers
REACTION OF SUBSTITUTED 1-HYDROXY-4-HYDROXYLAMINOIMIDAZOLIDIN-2-ONE WITH ARYL ISOCYANATES
E'pshtein, S.P.,Rukasov, A.F.,Tashchi, V.P.,Bashtrykov, P.M.,Putsykin, Yu.G.
, p. 897 - 900 (2007/10/02)
Various variants of reactions involving the carbamoylation of 1-hydroxy-3-(3'-chlorophenyl)-5,5-dimethyl-4-hydroxylaminoimidazolidin-2-one, which has three nucleophilic centers, viz., the N- and O-hydroxylamino groups and the O-hydroxyurea fragment of the
OXIDATION AND REDUCTION OF SUBSTITUTED 4-HYDROXYAMINO AND 4-OXIMINOIMIDAZOLIDIN-2-ONES
Epshtein, S. P.,Rukasov, A. F.,Tashchi, V. P.,Simonova, T. G.,Putsykin, Yu. G.
, p. 993 - 996 (2007/10/02)
4-Oximino-3-aryl(alkyl)-5,5-dimethylimidazolidin-2-ones were obtained by air oxidation of substituted 4-hydroxyaminoimidazolidin-2-ones in the presence of sodium ethoxide.In hydrochloric acid 4-oximino-3-(3',4'-dichlorophenyl)imidazolidin-2-one gives the corresponding hydantoin, whereas 4-oximino-3-(1'-phenylethyl)imidazolidin-2-one gives its E isomer with respect to the oxime group.The reduction of 4-oximino-3-alkylimidazolidin-2-ones with Raney alloy in 20percent NaOH or hydrogenation on a palladium catalyst leads to 4-imino derivatives, whereas reduction of 4-oximino-3-aryl-5,5-dimethylimidazolidin-2-ones that contain chlorine atoms in their aromatic rings with sodium in liquid ammonia leads to their dehalogenation.
