
Chemistry of Heterocyclic Compounds p. 496 - 501 (1991)
Update date:2022-08-05
Topics:
Pivovarenko, V. G.
Khilya, V. P.
It was shown that the reaction of α-(het)aryl-2,4-dihydroxy- and 2,4,6-trihydroxyacetophenones with acetoformic anhydride catalyzed by sodium formate is an effective method for the preparation of chromones containing a heteroaromatic residue at the 3-position.The yield of the chromone and the rate of the reaction increase with increase in the ?-deficiency of this residue or in the presence of a hydroxy group in the 6-position of the starting acetophenone.In the last case the method is also applicable to the preparation of the difficulty available 3-aryl-5,7-dihydroxychromones.Chromones with a nitrogen-containing residue are formed without the use of any catalyst.
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Doi:10.1080/10426500601096609
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