Abstract
There are no published data on chemical transformations of 2,5-substituted 1,2-oxazolidine-3,3-dicarbonitriles. With a view to elucidate the direction of hydrolysis of substituted 5-aryl-1,2-oxazolidine-3,3-dicarbonitriles we examined the reaction of 2-(2-nitro-1phenylethoxy)-5-phenyl-1,2-oxazolidine-3,3-dicarbonitrile (I) with dilute (1 : 1) hydrochloric acid. As a result, we obtained cinnamic acid III and benzoic acid (IV) which were formed, respectively, from the isoxazolidine fragment and side chain of compound I.
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