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5-Hydroxy-4- imidazolidines preparation

When l-hydroxy-3-imidazoline 3-oxides (263) are treated with HCl they dehydrate forming imidazole 3-oxides (Scheme 153) (73CHE1175). Reduction of 4//-imidazole N-oxides with borohydride leads to either 1-hydroxy-imidazolines or -imidazolidines, depending on the position of the oxide function. Under the same conditions 4//-imidazole 1,3-dioxides give 1,3-dihydroxyimidazolidines (76CHE1280). The 4iT-imidazole AT-oxides are prepared by heating 5,5-disubstituted l-acyloxy-3-imidazoline 3-oxides in vacuo. [Pg.455]


See other pages where 5-Hydroxy-4- imidazolidines preparation is mentioned: [Pg.209]    [Pg.209]    [Pg.450]    [Pg.85]    [Pg.342]    [Pg.412]    [Pg.182]    [Pg.93]    [Pg.93]   
See also in sourсe #XX -- [ Pg.68 , Pg.286 ]

See also in sourсe #XX -- [ Pg.68 , Pg.286 ]




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2- imidazolidines

2-Imidazolidine

5-Hydroxy-4- imidazolidines

Imidazolidin

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