丙二腈
化学
苯并呋喃
库仑法
亲核细胞
电化学
循环伏安法
分子内力
水溶液
迈克尔反应
亲核加成
有机化学
组合化学
电极
物理化学
催化作用
作者
Ali Reza Fakhari,Hamid Ahmar,Saied Saeed Hosseiny Davarani,Ahmad Shaabani,Sanaz Nikjah,Ali Maleki
标识
DOI:10.1080/00397911003629424
摘要
Abstract Abstract In this work, electrochemical oxidation of hydroquinones has been studied in the presence of malononitrile as a nucleophile in aqueous solution using cyclic voltammetry and controlled potential coulometry. The results indicate that the quinones derived from hydroquinones participate in Michael addition and then intramolecular nucleophilic addition to yield benzofuran derivatives. The electrochemical synthesis of these new 2-amino-3-cyano-benzofuran derivatives has been performed successfully at a carbon-rod electrode in an undivided cell in good to excellent yields at room temperature. Keywords: BenzofuranECECCC mechanismelectro-organic synthesishydroquinonemalononitrile ACKNOWLEDGMENT We gratefully acknowledge the financial support from the Research Council of Shahid Beheshti University.
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