Trifluoroacetylation-Induced Houben−Hoesch-Type Cyclization of Cyanoacetanilides: Increased Nucleophilicity of CN Groups
datasetposted on 16.04.2010 by Yusuke Kobayashi, Kosuke Katagiri, Isao Azumaya, Takashi Harayama
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Trifluoroacetic anhydride-mediated tandem trifluoroacetylation/cyclization of cyanoacetanilides proceeded efficiently under mild conditions to give 4-hydroxy-3-trifluoroacetylquinolin-2(1H)-ones in good yields. Isolation and direct observation of the reaction intermediates revealed that α-trifluoroacetylation resulted in the shortening of CN bonds and that the electron density of CN groups was high. A plausible reaction mechanism based on the results is also described.