Journal
SYNTHESIS-STUTTGART
Volume -, Issue 4, Pages 466-470Publisher
GEORG THIEME VERLAG KG
DOI: 10.1055/s-2002-20956
Keywords
Biginelli reaction; dihydropyrimidine-2(1H)-ones; nickel chloride hexahydrate; ferric chloride hexahydrate
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An efficient synthesis of 3.4-dihydropyrimidinones from the aldehyde. beta-keto ester and urea in ethanol. using ferric chloride hexahydrate or nickel chloride hexahydrate as the catalyst, is described. Compared with the classical Biginelli reaction conditions, this new method has the advantage of excellent yields (53-97%) and short reaction time (4-5 hours).
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