Manganese‐Catalyzed β‐Methylation of Alcohols by Methanol
We report an earth‐abundant‐metal‐catalyzed double and single methylation of alcohols. A manganese catalyst, which operates at low catalyst loadings and short reaction times, mediates these reactions efficiently. A broad scope of primary and secondary alcohols, including purely aliphatic examples, a...
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Veröffentlicht in: | Angewandte Chemie 2020-01, Vol.132 (4), p.1501-1506 |
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description | We report an earth‐abundant‐metal‐catalyzed double and single methylation of alcohols. A manganese catalyst, which operates at low catalyst loadings and short reaction times, mediates these reactions efficiently. A broad scope of primary and secondary alcohols, including purely aliphatic examples, and 1,2‐aminoalcohols can be methylated. Furthermore, alcohol methylation for the synthesis of pharmaceuticals has been demonstrated. The catalyst system tolerates many functional groups among them hydrogenation‐sensitive examples and upscaling is easily achieved. Mechanistic investigations are indicative of a borrowing hydrogen or hydrogen autotransfer mechanism involving a bimetallic K‐Mn catalyst. The catalyst accepts hydrogen as a proton and a hydride from alcohols efficiently and reacts with a chalcone via hydride transfer.
Einzel oder Doppel? Ein Mn‐basierter Katalysator ermöglicht die effiziente Einzelmethylierung sekundärer Kohlenstoffatome und Doppelmethylierung primärer Kohlenstoffatome von primären und sekundären Alkoholen, einschließlich rein aliphatischen Beispielen. Der Katalysator toleriert viele funktionelle Gruppen, agiert bei niedrigen Katalysatorbeladungen sowie kurzen Reaktionszeiten und ermöglicht einfache Maßstabsvergrößerung. |
doi_str_mv | 10.1002/ange.201912055 |
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Einzel oder Doppel? Ein Mn‐basierter Katalysator ermöglicht die effiziente Einzelmethylierung sekundärer Kohlenstoffatome und Doppelmethylierung primärer Kohlenstoffatome von primären und sekundären Alkoholen, einschließlich rein aliphatischen Beispielen. Der Katalysator toleriert viele funktionelle Gruppen, agiert bei niedrigen Katalysatorbeladungen sowie kurzen Reaktionszeiten und ermöglicht einfache Maßstabsvergrößerung.</description><identifier>ISSN: 0044-8249</identifier><identifier>EISSN: 1521-3757</identifier><identifier>DOI: 10.1002/ange.201912055</identifier><language>eng</language><publisher>Weinheim: Wiley Subscription Services, Inc</publisher><subject>Alcohol ; Alcohols ; Aliphatic compounds ; Alkohole ; Bimetals ; Catalysts ; Chemistry ; Functional groups ; Hydrides ; Hydrogen ; Hydrogen storage ; Mangan ; Manganese ; Methylation ; Methylierung ; Nachhaltige Chemie ; Wasserstoff leihen</subject><ispartof>Angewandte Chemie, 2020-01, Vol.132 (4), p.1501-1506</ispartof><rights>2020 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA.</rights><rights>2020. This article is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2025-1106a0237412ff0bc143206a0e2fe182dfea5a8222db2be16fd1c4af344ed5ae3</citedby><cites>FETCH-LOGICAL-c2025-1106a0237412ff0bc143206a0e2fe182dfea5a8222db2be16fd1c4af344ed5ae3</cites><orcidid>0000-0002-9138-4155</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%2Fange.201912055$$EPDF$$P50$$Gwiley$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fange.201912055$$EHTML$$P50$$Gwiley$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids></links><search><creatorcontrib>Schlagbauer, Martin</creatorcontrib><creatorcontrib>Kallmeier, Fabian</creatorcontrib><creatorcontrib>Irrgang, Torsten</creatorcontrib><creatorcontrib>Kempe, Rhett</creatorcontrib><title>Manganese‐Catalyzed β‐Methylation of Alcohols by Methanol</title><title>Angewandte Chemie</title><description>We report an earth‐abundant‐metal‐catalyzed double and single methylation of alcohols. A manganese catalyst, which operates at low catalyst loadings and short reaction times, mediates these reactions efficiently. A broad scope of primary and secondary alcohols, including purely aliphatic examples, and 1,2‐aminoalcohols can be methylated. Furthermore, alcohol methylation for the synthesis of pharmaceuticals has been demonstrated. The catalyst system tolerates many functional groups among them hydrogenation‐sensitive examples and upscaling is easily achieved. Mechanistic investigations are indicative of a borrowing hydrogen or hydrogen autotransfer mechanism involving a bimetallic K‐Mn catalyst. The catalyst accepts hydrogen as a proton and a hydride from alcohols efficiently and reacts with a chalcone via hydride transfer.
Einzel oder Doppel? Ein Mn‐basierter Katalysator ermöglicht die effiziente Einzelmethylierung sekundärer Kohlenstoffatome und Doppelmethylierung primärer Kohlenstoffatome von primären und sekundären Alkoholen, einschließlich rein aliphatischen Beispielen. Der Katalysator toleriert viele funktionelle Gruppen, agiert bei niedrigen Katalysatorbeladungen sowie kurzen Reaktionszeiten und ermöglicht einfache Maßstabsvergrößerung.</description><subject>Alcohol</subject><subject>Alcohols</subject><subject>Aliphatic compounds</subject><subject>Alkohole</subject><subject>Bimetals</subject><subject>Catalysts</subject><subject>Chemistry</subject><subject>Functional groups</subject><subject>Hydrides</subject><subject>Hydrogen</subject><subject>Hydrogen storage</subject><subject>Mangan</subject><subject>Manganese</subject><subject>Methylation</subject><subject>Methylierung</subject><subject>Nachhaltige Chemie</subject><subject>Wasserstoff leihen</subject><issn>0044-8249</issn><issn>1521-3757</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><recordid>eNqFkMFKw0AQhhdRsFavngOeU2dnd5vmIpRSq9DqRc_LJpm1LWu2ZlMknvoIPosP4kP4JCZU9CgMDDPzf__Az9g5hwEHwEtTPtEAgaccQakD1uMKeSwSlRyyHoCU8QhlesxOQlgDwBCTtMeuFi1mSgr0tXufmNq45o2K6POjHRdULxtn6pUvI2-jscv90rsQZU3UnUzp3Sk7ssYFOvvpffZ4PX2Y3MTz-9ntZDyPcwRUMecwNIAikRythSznUmC3IrTER1hYMsqMELHIMCM-tAXPpbFCSiqUIdFnF3vfTeVfthRqvfbbqmxfahSyrSRB0aoGe1Ve-RAqsnpTrZ5N1WgOustIdxnp34xaIN0DrytHzT9qPb6bTf_YbyO3bOo</recordid><startdate>20200120</startdate><enddate>20200120</enddate><creator>Schlagbauer, Martin</creator><creator>Kallmeier, Fabian</creator><creator>Irrgang, Torsten</creator><creator>Kempe, Rhett</creator><general>Wiley Subscription Services, Inc</general><scope>24P</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope><orcidid>https://orcid.org/0000-0002-9138-4155</orcidid></search><sort><creationdate>20200120</creationdate><title>Manganese‐Catalyzed β‐Methylation of Alcohols by Methanol</title><author>Schlagbauer, Martin ; Kallmeier, Fabian ; Irrgang, Torsten ; Kempe, Rhett</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2025-1106a0237412ff0bc143206a0e2fe182dfea5a8222db2be16fd1c4af344ed5ae3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Alcohol</topic><topic>Alcohols</topic><topic>Aliphatic compounds</topic><topic>Alkohole</topic><topic>Bimetals</topic><topic>Catalysts</topic><topic>Chemistry</topic><topic>Functional groups</topic><topic>Hydrides</topic><topic>Hydrogen</topic><topic>Hydrogen storage</topic><topic>Mangan</topic><topic>Manganese</topic><topic>Methylation</topic><topic>Methylierung</topic><topic>Nachhaltige Chemie</topic><topic>Wasserstoff leihen</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Schlagbauer, Martin</creatorcontrib><creatorcontrib>Kallmeier, Fabian</creatorcontrib><creatorcontrib>Irrgang, Torsten</creatorcontrib><creatorcontrib>Kempe, Rhett</creatorcontrib><collection>Wiley Online Library Open Access</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Angewandte Chemie</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Schlagbauer, Martin</au><au>Kallmeier, Fabian</au><au>Irrgang, Torsten</au><au>Kempe, Rhett</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Manganese‐Catalyzed β‐Methylation of Alcohols by Methanol</atitle><jtitle>Angewandte Chemie</jtitle><date>2020-01-20</date><risdate>2020</risdate><volume>132</volume><issue>4</issue><spage>1501</spage><epage>1506</epage><pages>1501-1506</pages><issn>0044-8249</issn><eissn>1521-3757</eissn><abstract>We report an earth‐abundant‐metal‐catalyzed double and single methylation of alcohols. A manganese catalyst, which operates at low catalyst loadings and short reaction times, mediates these reactions efficiently. A broad scope of primary and secondary alcohols, including purely aliphatic examples, and 1,2‐aminoalcohols can be methylated. Furthermore, alcohol methylation for the synthesis of pharmaceuticals has been demonstrated. The catalyst system tolerates many functional groups among them hydrogenation‐sensitive examples and upscaling is easily achieved. Mechanistic investigations are indicative of a borrowing hydrogen or hydrogen autotransfer mechanism involving a bimetallic K‐Mn catalyst. The catalyst accepts hydrogen as a proton and a hydride from alcohols efficiently and reacts with a chalcone via hydride transfer.
Einzel oder Doppel? Ein Mn‐basierter Katalysator ermöglicht die effiziente Einzelmethylierung sekundärer Kohlenstoffatome und Doppelmethylierung primärer Kohlenstoffatome von primären und sekundären Alkoholen, einschließlich rein aliphatischen Beispielen. Der Katalysator toleriert viele funktionelle Gruppen, agiert bei niedrigen Katalysatorbeladungen sowie kurzen Reaktionszeiten und ermöglicht einfache Maßstabsvergrößerung.</abstract><cop>Weinheim</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1002/ange.201912055</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0002-9138-4155</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Alcohol Alcohols Aliphatic compounds Alkohole Bimetals Catalysts Chemistry Functional groups Hydrides Hydrogen Hydrogen storage Mangan Manganese Methylation Methylierung Nachhaltige Chemie Wasserstoff leihen |
title | Manganese‐Catalyzed β‐Methylation of Alcohols by Methanol |
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