α-Diketone類によるGuanidine類の反応(第2報^<1)>)1-Phenylpropane-1,2-dioneおよびBenzilによる1,1-Pentamethyleneguanidine, Benzamidineの反応生成物の構造とVoges-Proskauer反応における呈色との関係について^<2,3)>

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The products from the positive Voges-Proskauer reaction namely, the reactions of 1-phenylpropane-1,2-dione (PPD) with 1,1-pentamethyleneguanidine (PMG), and those from the negative Voges-Proskauer reaction, namely the reactions of benzil with PMG, PPD with benzamidine, and of benzil with benzamidine were isolated, and the relation between the structural difference in these products and their color developments was elucidated. The reaction of PMG with PPD afforded 4-hydroxy-4-methyl-5-phenyl-2-piperidino-4H-imidazole [Ic], which is known as the intermediate in the Voges-Proskauer reaction. The reactions of PMG with benzil, benzamidine with PPD, and benzamidine with benzil afforded 2,4,4/2,5,5-trisubstituted-2-imidazolin-4/5-one-s [II, IV, V] and 4-hydroxy-4,5-diphenyl-2-piperidino-4H-imidazole [III], respectively. It was found that II, IV, and V were formed through the benzilic acid rearrangement, while the intramolecular rearrangement was not involved in the formation of III. II, IV, and V did not react to give any color development in the presence of alkali, but III which had a similar skeleton to that of I_c gave II with an intramolecular rearrangement. Since I_c gave the pigments (A, B, and C), whose structures were already elucidated, by the release of formaldehyde from 4-hydroxy and 4-methyl groups of 4H-imidazole or the reaction with 1-naphthol in the presence of alkali, this reaction process was found to be of importance for exhibiting the positive Voges-Proskauer reaction. A tautomerism was found between IV and V by examination of their IR spectra.
公益社団法人日本薬学会の論文
1977-03-25

α-Diketone類によるGuanidine類の反応(第2報^<1)>)1-Phenylpropane-1,2-dioneおよびBenzilによる1,1-Pentamethyleneguanidine, Benzamidineの反応生成物の構造とVoges-Proskauer反応における呈色との関係について^<2,3)>

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