Preparative methods were developed for the synthesis of 5-(N-tosylaminomethyl)furfuryl alcohols, and their behavior during the action of acidic catalysts was studied. It was established that the furan ring of these compounds is stable in the presence of orthophosphoric acid in glacial acetic acid and that their hydroxyl and N-tosylaminomethyl groups are involved in the transformations.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 5, pp. 671-679, May, 2009.
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Stroganova, T.A., Butin, A.V. Synthesis and some transformations of 5-(N-tosylaminomethyl)furfuryl alcohols. Chem Heterocycl Comp 45, 524–530 (2009). https://doi.org/10.1007/s10593-009-0302-y
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DOI: https://doi.org/10.1007/s10593-009-0302-y