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首页> 外文期刊>Beilstein journal of organic chemistry. >Electrochemically modified Corey–Fuchs reaction for the synthesis of arylalkynes. The case of 2-(2,2-dibromovinyl)naphthalene
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Electrochemically modified Corey–Fuchs reaction for the synthesis of arylalkynes. The case of 2-(2,2-dibromovinyl)naphthalene

机译:电化学修饰的Corey-Fuchs反应,用于合成芳基炔烃。 2-(2,2-二溴乙烯基)萘的情况

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摘要

The electrochemical reduction of 2-(2,2-dibromovinyl)naphthalene in a DMF solution (Pt cathode) yields selectively 2-ethynylnaphthalene or 2-(bromoethynyl)naphthalene in high yields, depending on the electrolysis conditions. In particular, by simply changing the working potential and the supporting electrolyte, the reaction can be directed towards the synthesis of the terminal alkyne (Et4NBF4) or the bromoalkyne (NaClO4). This study allowed to establish that 2-(bromoethynyl)naphthalene can be converted into 2-ethynylnaphthalene by cathodic reduction.
机译:根据电解条件,在DMF溶液(铂阴极)中对2-(2,2-二溴乙烯基)萘进行电化学还原可选择性地以高产率选择性生成2-乙炔基萘或2-(溴乙炔基)萘。特别是,通过简单地改变工作电位和支持电解质,该反应可以直接用于末端炔烃(Et 4 NBF 4 )或溴炔烃( NaClO 4 )。该研究允许建立2-(溴乙炔基)萘可以通过阴极还原转化为2-乙炔基萘。

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