期刊
SYNTHESIS-STUTTGART
卷 -, 期 12, 页码 1933-1937出版社
GEORG THIEME VERLAG KG
DOI: 10.1055/s-2008-1067079
关键词
tandem reactions; electrocatalysis; Knoevenagel reaction; Michael addition; pyrazolone
An electrochemically induced catalytic tandem Knoevenagel-Michael reaction of two equivalents of 5-methyl-2-phenyl-2,4-dihydro-3H-pyrazol-3-one with various aromatic aldehydes in ethanol in an undivided cell in the presence of sodium bromide as an electrolyte results in the formation of the corresponding 4,4'-(arylmethylene)bis(1 H-pyrazol-5-ols) in 80-96% yields. The application of this efficient electrocatalytic method to the synthesis of biologically prominent 4,4'-(arylmethylene)bis(1H-pyrazol-5-ols) represents a facile and convenient approach to the realization of the tandem Knoevenagel-Michael reaction.
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