Manganese(III)-Mediated formylation of aromatic compounds in the presence of malonic acid.
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概要
- 論文の詳細を見る
The reaction of naphthalenes with malonic acid in the presence of manganese(III) acetate gives naphthalenecarbaldehydes and naphthalenecarboxylic acids. Similar reactions of anthracene, pyrene, and methoxybenzenes also yield formylated and carboxylated products. It was found that the formyl group introduced to the aromatic ring was not derived from carboxymethyl radical generated directly by the thermolysis of manganese(III) acetate, but from a dicarboxymethyl radical formed by the interaction of malonic acid and manganese(III) acetate. In addition, it was also found that the dicarboxymethyl radicals attacked the position of the highest electron density on the aromatic ring and that this formylation was effective when the ionization potential of the aromatic compound was lower than 7.8 eV.
- 公益社団法人 日本化学会の論文
著者
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KUROSAWA Kazu
Department of Chemistry, Faculty of Science, Kumamoto University
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Kurosawa Kazu
Department Of Chemistry Faculty Of Science Kumamoto University
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Tsunoda Katsunori
Department Of Applied Chemistry Faculty Of Science Science University Of Tokyo
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Nishino Hiroshi
Department Of Applied Chemistry National Defense Academy
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