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Electrochemical Fluorination of Dithiocarbonates Using a Triarylamine Mediator
Electrochemical oxidation of O‐(4‐chlorobenzyl) S‐methyl dithiocarbonate using tris(2,4‐dibromophenyl)amine as a redox mediator was studied by cyclic voltammetric measurements. The triarylamine mediated anodic fluorodesulfurization of O‐(4‐chlorobenzyl) and O‐(4‐bromobenzyl) S‐methyl dithiocarbonate...
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Published in: | Electroanalysis (New York, N.Y.) N.Y.), 2021-11, Vol.33 (11), p.2296-2301 |
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container_title | Electroanalysis (New York, N.Y.) |
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creator | Okuda, Hirokazu Taniguchi, Kohei Inagi, Shinsuke Fuchigami, Toshio |
description | Electrochemical oxidation of O‐(4‐chlorobenzyl) S‐methyl dithiocarbonate using tris(2,4‐dibromophenyl)amine as a redox mediator was studied by cyclic voltammetric measurements. The triarylamine mediated anodic fluorodesulfurization of O‐(4‐chlorobenzyl) and O‐(4‐bromobenzyl) S‐methyl dithiocarbonates provided 4‐chloro‐ and 4‐bromobenzyl fluorides, respectively in moderate yields. On the other hand, similar anodic fluorination of O‐(2‐phenethyl) S‐octyl dithiocarbonate and O‐(4‐bromophenyl) S‐methyl dithiocarbonate afforded 2‐phenethyl trifluoromethyl ether and difluoro(methylthio)methyl 4‐bromophenyl ether, respectively. Mechanistic aspects are also discussed. |
doi_str_mv | 10.1002/elan.202100070 |
format | article |
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The triarylamine mediated anodic fluorodesulfurization of O‐(4‐chlorobenzyl) and O‐(4‐bromobenzyl) S‐methyl dithiocarbonates provided 4‐chloro‐ and 4‐bromobenzyl fluorides, respectively in moderate yields. On the other hand, similar anodic fluorination of O‐(2‐phenethyl) S‐octyl dithiocarbonate and O‐(4‐bromophenyl) S‐methyl dithiocarbonate afforded 2‐phenethyl trifluoromethyl ether and difluoro(methylthio)methyl 4‐bromophenyl ether, respectively. Mechanistic aspects are also discussed.</description><identifier>ISSN: 1040-0397</identifier><identifier>EISSN: 1521-4109</identifier><identifier>DOI: 10.1002/elan.202100070</identifier><language>eng</language><subject>Benzyl fluoride ; Dithiocarbonate ; Electrochemical fluorodesulfurization ; Fluoroether ; Triarylamine mediator</subject><ispartof>Electroanalysis (New York, N.Y.), 2021-11, Vol.33 (11), p.2296-2301</ispartof><rights>2021 Wiley‐VCH GmbH</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2890-a3dc738f97a551b2fb92de24d87ce6bd424e6622c2ea1fcf941f425d1c59a7c3</citedby><cites>FETCH-LOGICAL-c2890-a3dc738f97a551b2fb92de24d87ce6bd424e6622c2ea1fcf941f425d1c59a7c3</cites><orcidid>0000-0002-1905-5656</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Okuda, Hirokazu</creatorcontrib><creatorcontrib>Taniguchi, Kohei</creatorcontrib><creatorcontrib>Inagi, Shinsuke</creatorcontrib><creatorcontrib>Fuchigami, Toshio</creatorcontrib><title>Electrochemical Fluorination of Dithiocarbonates Using a Triarylamine Mediator</title><title>Electroanalysis (New York, N.Y.)</title><description>Electrochemical oxidation of O‐(4‐chlorobenzyl) S‐methyl dithiocarbonate using tris(2,4‐dibromophenyl)amine as a redox mediator was studied by cyclic voltammetric measurements. The triarylamine mediated anodic fluorodesulfurization of O‐(4‐chlorobenzyl) and O‐(4‐bromobenzyl) S‐methyl dithiocarbonates provided 4‐chloro‐ and 4‐bromobenzyl fluorides, respectively in moderate yields. On the other hand, similar anodic fluorination of O‐(2‐phenethyl) S‐octyl dithiocarbonate and O‐(4‐bromophenyl) S‐methyl dithiocarbonate afforded 2‐phenethyl trifluoromethyl ether and difluoro(methylthio)methyl 4‐bromophenyl ether, respectively. Mechanistic aspects are also discussed.</description><subject>Benzyl fluoride</subject><subject>Dithiocarbonate</subject><subject>Electrochemical fluorodesulfurization</subject><subject>Fluoroether</subject><subject>Triarylamine mediator</subject><issn>1040-0397</issn><issn>1521-4109</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNqFkD1PwzAQhi0EEqWwMvsPpNgXJ6nHqqSAVMpS5ujinKmRGyM7CPXfk6oIRqb70PucTg9jt1LMpBBwRx77GQgYB1GJMzaRBchMSaHPx14okYlcV5fsKqX3MaJLpSdsU3syQwxmR3tn0POV_wzR9Ti40PNg-b0bdi4YjG0Yl5T4a3L9G0e-jQ7jwePe9cSfqXM4hHjNLiz6RDc_dcq2q3q7fMzWLw9Py8U6MzDXIsO8M1U-t7rCopAt2FZDR6C6eWWobDsFisoSwAChtMZqJa2CopOm0FiZfMpmp7MmhpQi2eYjuv34TiNFc5TRHGU0vzJGQJ-AL-fp8E-6qdeLzR_7Dbo0ZRk</recordid><startdate>202111</startdate><enddate>202111</enddate><creator>Okuda, Hirokazu</creator><creator>Taniguchi, Kohei</creator><creator>Inagi, Shinsuke</creator><creator>Fuchigami, Toshio</creator><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0002-1905-5656</orcidid></search><sort><creationdate>202111</creationdate><title>Electrochemical Fluorination of Dithiocarbonates Using a Triarylamine Mediator</title><author>Okuda, Hirokazu ; Taniguchi, Kohei ; Inagi, Shinsuke ; Fuchigami, Toshio</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2890-a3dc738f97a551b2fb92de24d87ce6bd424e6622c2ea1fcf941f425d1c59a7c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Benzyl fluoride</topic><topic>Dithiocarbonate</topic><topic>Electrochemical fluorodesulfurization</topic><topic>Fluoroether</topic><topic>Triarylamine mediator</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Okuda, Hirokazu</creatorcontrib><creatorcontrib>Taniguchi, Kohei</creatorcontrib><creatorcontrib>Inagi, Shinsuke</creatorcontrib><creatorcontrib>Fuchigami, Toshio</creatorcontrib><collection>CrossRef</collection><jtitle>Electroanalysis (New York, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Okuda, Hirokazu</au><au>Taniguchi, Kohei</au><au>Inagi, Shinsuke</au><au>Fuchigami, Toshio</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Electrochemical Fluorination of Dithiocarbonates Using a Triarylamine Mediator</atitle><jtitle>Electroanalysis (New York, N.Y.)</jtitle><date>2021-11</date><risdate>2021</risdate><volume>33</volume><issue>11</issue><spage>2296</spage><epage>2301</epage><pages>2296-2301</pages><issn>1040-0397</issn><eissn>1521-4109</eissn><abstract>Electrochemical oxidation of O‐(4‐chlorobenzyl) S‐methyl dithiocarbonate using tris(2,4‐dibromophenyl)amine as a redox mediator was studied by cyclic voltammetric measurements. The triarylamine mediated anodic fluorodesulfurization of O‐(4‐chlorobenzyl) and O‐(4‐bromobenzyl) S‐methyl dithiocarbonates provided 4‐chloro‐ and 4‐bromobenzyl fluorides, respectively in moderate yields. On the other hand, similar anodic fluorination of O‐(2‐phenethyl) S‐octyl dithiocarbonate and O‐(4‐bromophenyl) S‐methyl dithiocarbonate afforded 2‐phenethyl trifluoromethyl ether and difluoro(methylthio)methyl 4‐bromophenyl ether, respectively. Mechanistic aspects are also discussed.</abstract><doi>10.1002/elan.202100070</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0002-1905-5656</orcidid></addata></record> |
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subjects | Benzyl fluoride Dithiocarbonate Electrochemical fluorodesulfurization Fluoroether Triarylamine mediator |
title | Electrochemical Fluorination of Dithiocarbonates Using a Triarylamine Mediator |
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