Abstract
The reaction of β-diethylaminoethyl chlorodiphenylacetate with ethanolamine has given β-diethylaminoethyl β-aminoethoxydiphenylacetate, the reaction of which with phenyl isothiocyanate followed by condensation with monochloroacetic acid has led to a derivative of a disubstituted thiazolidin-4-one, whose structure has been shown by hydroolytic cleavage. A number of arylidene derivatives of thiazolidin-4-one has been obtained. Their UV spectra agree with their structures.
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Yurzhenko, S.A., Turkevich, N.M. Synthesis and reactions of β-Diethylaminoethyl β-Aminoethoxydiphenylacetate. Chem Heterocycl Compd 6, 324–326 (1970). https://doi.org/10.1007/BF00471233
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DOI: https://doi.org/10.1007/BF00471233