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First synthesis of unexpected functionalized trifluoromethylated 8-oxa-2,4-diazaspiro[5.5]undecanes via one-pot MCRs†
Jia Li,Wei Shi,WenXin Yang,ZhangPing Kang,Min Zhang
RSC Advances Pub Date : 06/11/2014 00:00:00 , DOI:10.1039/C4RA03199G
Abstract

Ethyl-7,11-diaryl-9-hydroxy-1,3,5-trioxo-9-(trifluoromethyl)-8-oxa-2,4-diazaspiro[5.5]undecane-10-carboxylate derivatives (4) were synthesized from barbituric acid, aromatic aldehydes and ethyl 4,4,4-trifluoro-3-oxobutanoate via a one-pot, multi-component reaction catalyzed by Et3N. The effect of catalyst and temperature on reaction efficiency and yield was investigated. In addition, the treatment of 4 with SOCl2/pyridine in the solvent CH3CN afforded the corresponding dehydrated products 5. A plausible reaction mechanism for the formation of compounds 4 was presented.

Graphical abstract: First synthesis of unexpected functionalized trifluoromethylated 8-oxa-2,4-diazaspiro[5.5]undecanes via one-pot MCRs
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