Abstract
By reductive amination, starting from furfural, 5-methylfurfural, β-(2-furyl)acrolein, and monoethanolamine, we have obtained N-furfurylaminoethanol, N-(5-methyl-2-furfuryl)aminoethanol, and N-[1-(α-furyl)-3-propyl]aminoethanol. By reductive amination combined with the subsequent hydrogenation of the furan ring we have obtained N-tetrahydrofurfurylaminoethanol and N-(5-methyltetrahydro-2-furfuryl)aminoethanol.
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For part XXXIII, see [1].
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Ponomarev, A.A., Zadumina, E.A., Markushina, I.A. et al. Furan compounds. Chem Heterocycl Compd 4, 442–443 (1971). https://doi.org/10.1007/BF00486751
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DOI: https://doi.org/10.1007/BF00486751