Reactions of diazoalkanes with isocyanates. Synthesis of imidazolidine-2, 4-diones, oxindoles, and oxazolidinones
JB Fulton, J Warkentin
Index: Fulton, Janet B.; Warkentin, John Canadian Journal of Chemistry, 1987 , vol. 65, p. 1177 - 1184
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Citation Number: 7
Abstract
Thermolysis of a 5, 5-dialkyl-Δ3-1, 3, 4-oxadiazolin-2-one in nitrobenzene containing an aryl isocyanate at 150° C affords a 1, 3-diaryl-5, 5-dialkylimidazolidine-2, 4-dione, an N- arylcarbamoyl-3, 3-dialkyloxindole, and a 3-aryl-2-arylimino-5, 5-dialkyl-1, 3-oxazolidin-4- one. Those products arise from attack of a diazoalkane, generated in situ from the oxadiazolinone by thermal cycloreversion, on the isocyanate function. Two imidazolidine ...
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[Lee,S.L. et al. Canadian Journal of Chemistry, 1972 , vol. 50, p. 2326 - 2331]