Abstract
The optimum conditions were found for the condensation of glycerol with furfural. It was shown that the reaction of glycerol with furfural gives a mixture of the cis and trans isomers of five- and six-membered furan 1,3-dioxacyclanes. The cis- and trans-5-hydroxy-2-furyl-1,3-dioxanes were isolated by column chromatography, and their stereochemical structure was established by IR and NMR spectroscopy.
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Gromachevskaya, E.V., Kvitkovsky, F.V., Usova, E.B. et al. Investigation in the Area of Furan Acetal Compounds. 13. Synthesis and Structure of 1,3-Dioxacyclanes Based on Furfural and Glycerol. Chemistry of Heterocyclic Compounds 40, 979–985 (2004). https://doi.org/10.1023/B:COHC.0000046685.17653.c4
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DOI: https://doi.org/10.1023/B:COHC.0000046685.17653.c4