Synthesis of Aryl Carboxylic Acids through Ambient Electro-oxidation of Arylacetylenes

IF 2.2 4区 化学 Q2 CHEMISTRY, ORGANIC Synthesis-Stuttgart Pub Date : 2023-10-18 DOI:10.1055/s-0041-1738456
Yanhua Zhang, Hongyan Yuan, Manxin Sun, Tong Zhang, Guohao Wu
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Abstract

Abstract An efficient and environment-friendly synthesis of aryl carboxylic acids through the ambient electro-oxidation of the arylacetylenes is demonstrated. The reaction proceeds smoothly at certain applied potentials in a mixed solution of acetonitrile and water with potassium peroxymonosulfate (Oxone) as the additive. The isolated yields of the desired products are good up to 90%, and the reaction exhibits excellent functional-group tolerance. In this electrochemical system, transition metal catalysts, extra acids/bases, and high temperature are not required. This method may open up a pathway for the synthesis of carboxylic acids by the electrochemistry strategy.
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芳基乙炔环境电氧化合成芳基羧酸的研究
摘要研究了芳基乙炔在环境电氧化条件下高效、环保地合成芳基羧酸的方法。在乙腈和水的混合溶液中,以过氧单硫酸氢钾(氧酮)为添加剂,在一定的施加电位下,反应顺利进行。分离产物的收率可达90%以上,反应具有良好的官能团耐受性。在这种电化学系统中,不需要过渡金属催化剂、额外的酸/碱和高温。该方法为电化学合成羧酸开辟了新的途径。
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来源期刊
Synthesis-Stuttgart
Synthesis-Stuttgart 化学-有机化学
CiteScore
4.50
自引率
7.70%
发文量
435
审稿时长
1 months
期刊介绍: SYNTHESIS is an international full-paper journal devoted to the advancement of the science of chemical synthesis. It covers all fields of organic chemistry involving synthesis, including catalysis, organometallic, medicinal, biological, and photochemistry, but also related disciplines. SYNTHESIS provides dependable research results with detailed and reliable experimental procedures and full characterization of all important new products as well as scientific primary data.
期刊最新文献
Dealkenylative Functionalizations: Conversion of Alkene C(sp3)-C(sp2) Bonds into C(sp3)-X Bonds via Redox-Based Radical Processes. Aryl Annulation: A Powerful Simplifying Retrosynthetic Disconnection. Improved Syntheses of an Arseno-Fatty Acid (As-FA 362) and an Arseno-Hydrocarbon (As-HC 444). SYNFORM ISSUE 2023/12 Linked PDF of Table of Contents
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