Synthesis of 2-(1-Alkoxyvinyl)oxazolidines by Condensation of 2-Alkoxypropenals with 2-Aminoalkanols and Ring-Chain Tautomerism of the Products |
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| Authors: | Keiko N. A. Funtikova E. A. Stepanova L. G. Chuvashev Yu. A. Larina L. I. |
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| Affiliation: | (1) Favorskii Irkutsk Institute of Chemistry, Siberian Division, Russian Academy of Sciences, ul. Favorskogo 1, Irkutsk, 664033, Russia |
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| Abstract: | Reactions of 2-alkoxypropenals with 2-aminoalkanols afforded tautomeric mixtures of previously unknown 2-(1-alkoxyvinyl)oxazolidines and imino alcohols. The condensation takes 2 h at room temperature (89-100%) or 1-5 min under microwave irradiation. The tautomeric equilibrium shifts toward the open-chain structure with increase in the solvent polarity (CDCl3, CD2OD, DMSO-d6, D2O) and temperature. The presence of substituents in the oxazolidine ring raises the stability of the cyclic tautomer. |
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