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  • Alcohol mediated synthesis of 4-oxo-2-aryl-4H-chromene-3-carboxylate derivatives from 4-hydroxycoumarins.

Alcohol mediated synthesis of 4-oxo-2-aryl-4H-chromene-3-carboxylate derivatives from 4-hydroxycoumarins.

The Journal of organic chemistry (2012-07-20)
Manoj R Zanwar, Mustafa J Raihan, Sachin D Gawande, Veerababurao Kavala, Donala Janreddy, Chun-Wei Kuo, Ram Ambre, Ching-Fa Yao
ABSTRACT

The unusual alcohol mediated formation of 4-oxo-2-aryl-4H-chromene-3-carboxylate (flavone-3-carboxylate) derivatives from 4-hydroxycoumarins and β-nitroalkenes in an alcoholic medium is described. The transformation occurs via the in situ formation of a Michael adduct, followed by the alkoxide ion mediated rearrangement of the intermediate. The effect of the different alcohol and nonalcohol media on the reaction was investigated.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
trans-4-Methyl-β-nitrostyrene, 98%
Sigma-Aldrich
4-Hydroxycoumarin, 98%