Novel Non‐toxic and Non‐hazardous Solvent Systems for the Chemistry of Indoles: Use of a Sulfone‐containing Brønsted Acid Ionic Liquid Catalyst in Butyl Acetate
Dipolar and aprotic solvents are often required in acid‐catalyzed reactions, however, many of them are listed in solvent selection guides as not‐recommended due to their toxicity or explosivity. A catalytically functionalized ionic liquid, namely a sulfone‐containing imidazolium‐based Brønsted acid...
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creator | El‐Harairy, Ahmed Yiliqi Yue, Meie Fan, Weigang Popowycz, Florence Queneau, Yves Li, Minghao Gu, Yanlong |
description | Dipolar and aprotic solvents are often required in acid‐catalyzed reactions, however, many of them are listed in solvent selection guides as not‐recommended due to their toxicity or explosivity. A catalytically functionalized ionic liquid, namely a sulfone‐containing imidazolium‐based Brønsted acid ionic liquid, was synthesized. It alleviates the detrimental effect of classical dipolar aprotic solvents because this ionic liquid integrates the function of a dipolar aprotic solvent able to stabilize carbocation intermediates and the activating effect of a strong Brønsted acid on electrophiles. The use of this tailor‐made ionic liquid was exemplified in some transformation reactions of indoles, which proceeded with high yield and selectivity using a green and an industrially acceptable solvent, butyl acetate. The recyclability of the ionic liquid catalyst was also demonstrated.
Industrially acceptable: Dipolar and aprotic solvents are widely used in organic synthesis. These solvents are however generally toxic and hazardous. We created a new ionic liquid that allow the acid‐catalyzed reactions performed very well in green and an industrially acceptable solvent, butyl acetate. Indole transformations are model reactions to show the proof‐of‐the‐concept. |
doi_str_mv | 10.1002/cctc.201900784 |
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Industrially acceptable: Dipolar and aprotic solvents are widely used in organic synthesis. These solvents are however generally toxic and hazardous. We created a new ionic liquid that allow the acid‐catalyzed reactions performed very well in green and an industrially acceptable solvent, butyl acetate. Indole transformations are model reactions to show the proof‐of‐the‐concept.</description><identifier>ISSN: 1867-3880</identifier><identifier>ISSN: 1867-3899</identifier><identifier>EISSN: 1867-3899</identifier><identifier>DOI: 10.1002/cctc.201900784</identifier><language>eng</language><publisher>Weinheim: Wiley Subscription Services, Inc</publisher><subject>acid catalysis ; Acids ; Catalysis ; Catalysts ; Chemical reactions ; Chemical Sciences ; dipolar aprotic solvent ; green solvent ; indole transformation ; Indoles ; ionic liquid ; Ionic liquids ; Ions ; Organic chemistry ; Recyclability ; Selectivity ; Solvents ; Toxicity</subject><ispartof>ChemCatChem, 2019-09, Vol.11 (17), p.4403-4410</ispartof><rights>2019 Wiley‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3914-1692acd6dc8a1238d437f4a7a4e51b0a201a006418986d8e0a610ace0b1a92cf3</citedby><cites>FETCH-LOGICAL-c3914-1692acd6dc8a1238d437f4a7a4e51b0a201a006418986d8e0a610ace0b1a92cf3</cites><orcidid>0000-0003-4052-061X ; 0000-0002-0297-295X ; 0000-0002-7386-5190</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fcctc.201900784$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fcctc.201900784$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,314,776,780,881,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://udl.hal.science/hal-02193181$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>El‐Harairy, Ahmed</creatorcontrib><creatorcontrib>Yiliqi</creatorcontrib><creatorcontrib>Yue, Meie</creatorcontrib><creatorcontrib>Fan, Weigang</creatorcontrib><creatorcontrib>Popowycz, Florence</creatorcontrib><creatorcontrib>Queneau, Yves</creatorcontrib><creatorcontrib>Li, Minghao</creatorcontrib><creatorcontrib>Gu, Yanlong</creatorcontrib><title>Novel Non‐toxic and Non‐hazardous Solvent Systems for the Chemistry of Indoles: Use of a Sulfone‐containing Brønsted Acid Ionic Liquid Catalyst in Butyl Acetate</title><title>ChemCatChem</title><description>Dipolar and aprotic solvents are often required in acid‐catalyzed reactions, however, many of them are listed in solvent selection guides as not‐recommended due to their toxicity or explosivity. A catalytically functionalized ionic liquid, namely a sulfone‐containing imidazolium‐based Brønsted acid ionic liquid, was synthesized. It alleviates the detrimental effect of classical dipolar aprotic solvents because this ionic liquid integrates the function of a dipolar aprotic solvent able to stabilize carbocation intermediates and the activating effect of a strong Brønsted acid on electrophiles. The use of this tailor‐made ionic liquid was exemplified in some transformation reactions of indoles, which proceeded with high yield and selectivity using a green and an industrially acceptable solvent, butyl acetate. The recyclability of the ionic liquid catalyst was also demonstrated.
Industrially acceptable: Dipolar and aprotic solvents are widely used in organic synthesis. These solvents are however generally toxic and hazardous. We created a new ionic liquid that allow the acid‐catalyzed reactions performed very well in green and an industrially acceptable solvent, butyl acetate. Indole transformations are model reactions to show the proof‐of‐the‐concept.</description><subject>acid catalysis</subject><subject>Acids</subject><subject>Catalysis</subject><subject>Catalysts</subject><subject>Chemical reactions</subject><subject>Chemical Sciences</subject><subject>dipolar aprotic solvent</subject><subject>green solvent</subject><subject>indole transformation</subject><subject>Indoles</subject><subject>ionic liquid</subject><subject>Ionic liquids</subject><subject>Ions</subject><subject>Organic chemistry</subject><subject>Recyclability</subject><subject>Selectivity</subject><subject>Solvents</subject><subject>Toxicity</subject><issn>1867-3880</issn><issn>1867-3899</issn><issn>1867-3899</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNqFkUFuEzEYhUcIJEphy9oSKxYJtmc6Y7NLR0AjRWWRdm39tf8hrhy7tT0pw4ojcAuuwJ6bcBIcpQpLVvazvvd-26-qXjM6Z5Tyd1pnPeeUSUo70TypTphou1ktpHx63Av6vHqR0i2lray7s5Pq52XYoSOXwf_5_iOHr1YT8OZRb-AbRBPGRNbB7dBnsp5Sxm0iQ4gkb5D0G9zalONEwkCW3gSH6T25TrjXQNajG4LHEqWDz2C99V_Iefz9y5cYQxbaGrIMvgxd2fuxiB4yuDKDWE_Oxzy5wmCGjC-rZwO4hK8e19Pq-uOHq_5itvr8adkvVjNdS9bMWCs5aNMaLYDxWpim7oYGOmjwjN1QKN8D5e0NE1K0RiCFllHQSG8YSK6H-rR6e8jdgFN30W4hTiqAVReLldqfUc5kzQTbscK-ObB3MdyPmLK6DWP05XqKc8lb0XSMFmp-oHQMKUUcjrGMqn1xal-cOhZXDPJgeLAOp__Qqu-v-n_ev-GloVg</recordid><startdate>20190905</startdate><enddate>20190905</enddate><creator>El‐Harairy, Ahmed</creator><creator>Yiliqi</creator><creator>Yue, Meie</creator><creator>Fan, Weigang</creator><creator>Popowycz, Florence</creator><creator>Queneau, Yves</creator><creator>Li, Minghao</creator><creator>Gu, Yanlong</creator><general>Wiley Subscription Services, Inc</general><general>Wiley</general><scope>AAYXX</scope><scope>CITATION</scope><scope>1XC</scope><scope>VOOES</scope><orcidid>https://orcid.org/0000-0003-4052-061X</orcidid><orcidid>https://orcid.org/0000-0002-0297-295X</orcidid><orcidid>https://orcid.org/0000-0002-7386-5190</orcidid></search><sort><creationdate>20190905</creationdate><title>Novel Non‐toxic and Non‐hazardous Solvent Systems for the Chemistry of Indoles: Use of a Sulfone‐containing Brønsted Acid Ionic Liquid Catalyst in Butyl Acetate</title><author>El‐Harairy, Ahmed ; Yiliqi ; Yue, Meie ; Fan, Weigang ; Popowycz, Florence ; Queneau, Yves ; Li, Minghao ; Gu, Yanlong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3914-1692acd6dc8a1238d437f4a7a4e51b0a201a006418986d8e0a610ace0b1a92cf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>acid catalysis</topic><topic>Acids</topic><topic>Catalysis</topic><topic>Catalysts</topic><topic>Chemical reactions</topic><topic>Chemical Sciences</topic><topic>dipolar aprotic solvent</topic><topic>green solvent</topic><topic>indole transformation</topic><topic>Indoles</topic><topic>ionic liquid</topic><topic>Ionic liquids</topic><topic>Ions</topic><topic>Organic chemistry</topic><topic>Recyclability</topic><topic>Selectivity</topic><topic>Solvents</topic><topic>Toxicity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>El‐Harairy, Ahmed</creatorcontrib><creatorcontrib>Yiliqi</creatorcontrib><creatorcontrib>Yue, Meie</creatorcontrib><creatorcontrib>Fan, Weigang</creatorcontrib><creatorcontrib>Popowycz, Florence</creatorcontrib><creatorcontrib>Queneau, Yves</creatorcontrib><creatorcontrib>Li, Minghao</creatorcontrib><creatorcontrib>Gu, Yanlong</creatorcontrib><collection>CrossRef</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><jtitle>ChemCatChem</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>El‐Harairy, Ahmed</au><au>Yiliqi</au><au>Yue, Meie</au><au>Fan, Weigang</au><au>Popowycz, Florence</au><au>Queneau, Yves</au><au>Li, Minghao</au><au>Gu, Yanlong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Novel Non‐toxic and Non‐hazardous Solvent Systems for the Chemistry of Indoles: Use of a Sulfone‐containing Brønsted Acid Ionic Liquid Catalyst in Butyl Acetate</atitle><jtitle>ChemCatChem</jtitle><date>2019-09-05</date><risdate>2019</risdate><volume>11</volume><issue>17</issue><spage>4403</spage><epage>4410</epage><pages>4403-4410</pages><issn>1867-3880</issn><issn>1867-3899</issn><eissn>1867-3899</eissn><abstract>Dipolar and aprotic solvents are often required in acid‐catalyzed reactions, however, many of them are listed in solvent selection guides as not‐recommended due to their toxicity or explosivity. A catalytically functionalized ionic liquid, namely a sulfone‐containing imidazolium‐based Brønsted acid ionic liquid, was synthesized. It alleviates the detrimental effect of classical dipolar aprotic solvents because this ionic liquid integrates the function of a dipolar aprotic solvent able to stabilize carbocation intermediates and the activating effect of a strong Brønsted acid on electrophiles. The use of this tailor‐made ionic liquid was exemplified in some transformation reactions of indoles, which proceeded with high yield and selectivity using a green and an industrially acceptable solvent, butyl acetate. The recyclability of the ionic liquid catalyst was also demonstrated.
Industrially acceptable: Dipolar and aprotic solvents are widely used in organic synthesis. These solvents are however generally toxic and hazardous. We created a new ionic liquid that allow the acid‐catalyzed reactions performed very well in green and an industrially acceptable solvent, butyl acetate. Indole transformations are model reactions to show the proof‐of‐the‐concept.</abstract><cop>Weinheim</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1002/cctc.201900784</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0003-4052-061X</orcidid><orcidid>https://orcid.org/0000-0002-0297-295X</orcidid><orcidid>https://orcid.org/0000-0002-7386-5190</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | acid catalysis Acids Catalysis Catalysts Chemical reactions Chemical Sciences dipolar aprotic solvent green solvent indole transformation Indoles ionic liquid Ionic liquids Ions Organic chemistry Recyclability Selectivity Solvents Toxicity |
title | Novel Non‐toxic and Non‐hazardous Solvent Systems for the Chemistry of Indoles: Use of a Sulfone‐containing Brønsted Acid Ionic Liquid Catalyst in Butyl Acetate |
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