FIELD: chemistry.
SUBSTANCE: invention relates to a method for selective reduction of an aldehyde group to a methyl group in substituted furans to obtain 5-methyl-substituted furans of general formula (I), where R1 is selected from the group consisting of the following: a hydrogen atom, hydroxymethyl, alkyl, hydroxy group, aldehyde group, halogen atom, ester group, carboxyl, nitro group, amino group, amide, substituted amino group, alkoxy/ether bridges, sulphur derivatives, phosphorus derivatives, and an aryl and heteroaryl functional group; and R2 and R3 are selected from the group consisting of the following: a hydrogen atom, alkyl and aryl, where said method comprises the steps of: i) reacting an amine compound and an inorganic base with a substituted furfural of formula (II) in a solvent to obtain in situ the corresponding imine compound; ii) in situ reduction of the generated imine from step (i) under basic conditions in a solvent to obtain 5-methyl-substituted furans of general formula (I); iii) extraction of methyl-substituted furans of general formula (I).
EFFECT: proposed method is convenient, efficient and scalable.
13 cl, 9 ex
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Authors
Dates
2024-12-02—Published
2021-02-19—Filed