Abstract
Furfural oxidizes aliphatic and alicyclic alcohols at 70–100°C under the action of sodium alcoholate to aldehydes and ketones, and then participates in a crotonate condensation. At 0–10°C the alcohol is not oxidized but the adduct with alkoxide ion is oxidized to form an alkyl furoate.
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For Communication 3, see [1].
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 1, pp. 25–28, January, 1993.
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Shapiro, Y.M. Reactions of furan aldehydes 4. Oxidation-reduction reactions of furfural with monohydric alcohols. Chem Heterocycl Compd 29, 20–22 (1993). https://doi.org/10.1007/BF00528631
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DOI: https://doi.org/10.1007/BF00528631