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A Simple, Effective, Green Method for the Regioselective 3-Acylation of Unprotected Indoles
A fast and green method is developed for regioselective acylation of indoles in the 3-position without the need for protection of the NH position. The method is based on Friedel-Crafts acylation using acid anhydrides. The method has been optimized, and Y(OTf)₃ in catalytic amounts is found to be the...
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Published in: | Molecules (Basel, Switzerland) Switzerland), 2015-10, Vol.20 (10), p.19605-19619 |
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creator | Tran, Phuong Hoang Tran, Hai Ngoc Hansen, Poul Erik Do, Mai Hoang Ngoc Le, Thach Ngoc |
description | A fast and green method is developed for regioselective acylation of indoles in the 3-position without the need for protection of the NH position. The method is based on Friedel-Crafts acylation using acid anhydrides. The method has been optimized, and Y(OTf)₃ in catalytic amounts is found to be the best catalyst together with the commercially available ionic liquid [BMI]BF₄ (1-butyl-3-methylimidazolium tetrafluoro-borate) as solvent. The reaction is completed in a very short time using monomode microwave irradiation. The catalyst can be reused up to four times without significant loss of activity. A range of substituted indoles are investigated as substrates, and thirteen new compounds have been synthesized. |
doi_str_mv | 10.3390/molecules201019605 |
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The method is based on Friedel-Crafts acylation using acid anhydrides. The method has been optimized, and Y(OTf)₃ in catalytic amounts is found to be the best catalyst together with the commercially available ionic liquid [BMI]BF₄ (1-butyl-3-methylimidazolium tetrafluoro-borate) as solvent. The reaction is completed in a very short time using monomode microwave irradiation. The catalyst can be reused up to four times without significant loss of activity. A range of substituted indoles are investigated as substrates, and thirteen new compounds have been synthesized.</description><identifier>ISSN: 1420-3049</identifier><identifier>EISSN: 1420-3049</identifier><identifier>DOI: 10.3390/molecules201019605</identifier><identifier>PMID: 26516834</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Acids ; Acylation ; Catalysis ; Friedel-Crafts acylation ; Green Chemistry Technology ; indole derivatives ; Indoles - chemical synthesis ; Indoles - chemistry ; ionic liquids ; metal triflate ; microwave irradiation ; Microwaves ; Molecular Structure ; Solvents ; Stereoisomerism</subject><ispartof>Molecules (Basel, Switzerland), 2015-10, Vol.20 (10), p.19605-19619</ispartof><rights>Copyright MDPI AG 2015</rights><rights>2015 by the authors. 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c562t-13c157210d840b82973b88263cdaffdf186c812fd0837e69fa0e7390b02177033</citedby><cites>FETCH-LOGICAL-c562t-13c157210d840b82973b88263cdaffdf186c812fd0837e69fa0e7390b02177033</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1732946532/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1732946532?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25751,27922,27923,37010,37011,44588,53789,53791,74896</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26516834$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tran, Phuong Hoang</creatorcontrib><creatorcontrib>Tran, Hai Ngoc</creatorcontrib><creatorcontrib>Hansen, Poul Erik</creatorcontrib><creatorcontrib>Do, Mai Hoang Ngoc</creatorcontrib><creatorcontrib>Le, Thach Ngoc</creatorcontrib><title>A Simple, Effective, Green Method for the Regioselective 3-Acylation of Unprotected Indoles</title><title>Molecules (Basel, Switzerland)</title><addtitle>Molecules</addtitle><description>A fast and green method is developed for regioselective acylation of indoles in the 3-position without the need for protection of the NH position. 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A range of substituted indoles are investigated as substrates, and thirteen new compounds have been synthesized.</description><subject>Acids</subject><subject>Acylation</subject><subject>Catalysis</subject><subject>Friedel-Crafts acylation</subject><subject>Green Chemistry Technology</subject><subject>indole derivatives</subject><subject>Indoles - chemical synthesis</subject><subject>Indoles - chemistry</subject><subject>ionic liquids</subject><subject>metal triflate</subject><subject>microwave irradiation</subject><subject>Microwaves</subject><subject>Molecular Structure</subject><subject>Solvents</subject><subject>Stereoisomerism</subject><issn>1420-3049</issn><issn>1420-3049</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNplksFu1DAQQCMEoqXwAxyQJS4cCIzt2LEvSKuqtCsVIQE9cbAce7ybVRIvdlKpf4_plqqFk0eeN08z9lTVawofONfwcYwDumXAzIAC1RLEk-qYNgxqDo1--iA-ql7kvANgtKHieXXEpKBS8ea4-rki3_txP-B7chYCurm_LuF5QpzIF5y30ZMQE5m3SL7hpo8ZhwNEeL1yN4Od-ziRGMjVtE9xLjn0ZD350lp-WT0Ldsj46u48qa4-n_04vagvv56vT1eXtROSzTXljoqWUfCqgU4x3fJOKSa58zYEH6iSTlEWPCjeotTBArZl_q6M07bA-Um1Pnh9tDuzT_1o042Jtje3FzFtjE1z7wY0vtUA0GnWoGiC7TrNGUjLOqeE8N4V16eDa790I3qH05zs8Ej6ODP1W7OJ10ZyThWDInh3J0jx14J5NmOfHQ6DnTAu2dCWaS6gaVVB3_6D7uKSpvJUheJMN1JwVih2oFyKOScM981QMH_2wPy_B6XozcMx7kv-fjz_DWJKr0o</recordid><startdate>20151027</startdate><enddate>20151027</enddate><creator>Tran, Phuong Hoang</creator><creator>Tran, Hai Ngoc</creator><creator>Hansen, Poul Erik</creator><creator>Do, Mai Hoang Ngoc</creator><creator>Le, Thach Ngoc</creator><general>MDPI AG</general><general>MDPI</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20151027</creationdate><title>A Simple, Effective, Green Method for the Regioselective 3-Acylation of Unprotected Indoles</title><author>Tran, Phuong Hoang ; 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subjects | Acids Acylation Catalysis Friedel-Crafts acylation Green Chemistry Technology indole derivatives Indoles - chemical synthesis Indoles - chemistry ionic liquids metal triflate microwave irradiation Microwaves Molecular Structure Solvents Stereoisomerism |
title | A Simple, Effective, Green Method for the Regioselective 3-Acylation of Unprotected Indoles |
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