N-formylation and N-methylation of amines using metal-free N-heterocyclic carbene catalysts and CO2 as carbon source
This protocol describes the environmentally benign N -formylation and N -methylation of primary and secondary amines using carbon dioxide as the carbon source, hydrosilanes as reductants and N -heterocyclic carbenes as catalysts. N -formylation and N -methylation of amines are important reactions th...
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description | This protocol describes the environmentally benign
N
-formylation and
N
-methylation of primary and secondary amines using carbon dioxide as the carbon source, hydrosilanes as reductants and
N
-heterocyclic carbenes as catalysts.
N
-formylation and
N
-methylation of amines are important reactions that are used to produce a wide range of key intermediates and compounds. This protocol describes the environmentally benign
N
-formylation and
N
-methylation of primary and secondary amines using carbon dioxide (CO
2
) as the carbon source, hydrosilanes as reductants and
N
-heterocyclic carbenes (NHCs) as catalysts. Using CO
2
as a reagent has the advantage of low cost and negligible toxicity. However, the catalyst is air-sensitive and must be generated fresh before use; consequently, the techniques used to prepare and manipulate the catalyst are described. The synthetic approach described in this protocol does not use any toxic reagents; using the appropriate catalyst,
N
-formylated or
N
-methylated products can be obtained with high selectivity. The overall time for catalyst preparation and for conducting several catalytic reactions in parallel is 15–48 h, depending on the nature of the substrates. |
doi_str_mv | 10.1038/nprot.2016.175 |
format | Article |
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N
-formylation and
N
-methylation of primary and secondary amines using carbon dioxide as the carbon source, hydrosilanes as reductants and
N
-heterocyclic carbenes as catalysts.
N
-formylation and
N
-methylation of amines are important reactions that are used to produce a wide range of key intermediates and compounds. This protocol describes the environmentally benign
N
-formylation and
N
-methylation of primary and secondary amines using carbon dioxide (CO
2
) as the carbon source, hydrosilanes as reductants and
N
-heterocyclic carbenes (NHCs) as catalysts. Using CO
2
as a reagent has the advantage of low cost and negligible toxicity. However, the catalyst is air-sensitive and must be generated fresh before use; consequently, the techniques used to prepare and manipulate the catalyst are described. The synthetic approach described in this protocol does not use any toxic reagents; using the appropriate catalyst,
N
-formylated or
N
-methylated products can be obtained with high selectivity. The overall time for catalyst preparation and for conducting several catalytic reactions in parallel is 15–48 h, depending on the nature of the substrates.</description><identifier>ISSN: 1754-2189</identifier><identifier>EISSN: 1750-2799</identifier><identifier>DOI: 10.1038/nprot.2016.175</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>639/638/403/933 ; 639/638/77/889 ; Amines ; Analytical Chemistry ; Biological Techniques ; Carbenes ; Carbon dioxide ; Carbon sources ; Catalysis ; Catalysts ; Computational Biology/Bioinformatics ; Intermediates ; Life Sciences ; Ligands ; Methods ; Methylation ; Microarrays ; Organic Chemistry ; Precious metals ; Properties ; Protocol ; Reagents ; Reducing agents ; Selectivity ; Substrates ; Toxicity</subject><ispartof>Nature protocols, 2017-02, Vol.12 (2), p.417-428</ispartof><rights>Springer Nature Limited 2017</rights><rights>COPYRIGHT 2017 Nature Publishing Group</rights><rights>Copyright Nature Publishing Group Feb 2017</rights><rights>Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. 2017.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c501t-4a6e949d0434ed513d4fbc81b540b0700129bcd46116109620cbf147b20a2f633</citedby><cites>FETCH-LOGICAL-c501t-4a6e949d0434ed513d4fbc81b540b0700129bcd46116109620cbf147b20a2f633</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1038/nprot.2016.175$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1038/nprot.2016.175$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids></links><search><creatorcontrib>Bobbink, Felix D</creatorcontrib><creatorcontrib>Das, Shoubhik</creatorcontrib><creatorcontrib>Dyson, Paul J</creatorcontrib><title>N-formylation and N-methylation of amines using metal-free N-heterocyclic carbene catalysts and CO2 as carbon source</title><title>Nature protocols</title><addtitle>Nat Protoc</addtitle><description>This protocol describes the environmentally benign
N
-formylation and
N
-methylation of primary and secondary amines using carbon dioxide as the carbon source, hydrosilanes as reductants and
N
-heterocyclic carbenes as catalysts.
N
-formylation and
N
-methylation of amines are important reactions that are used to produce a wide range of key intermediates and compounds. This protocol describes the environmentally benign
N
-formylation and
N
-methylation of primary and secondary amines using carbon dioxide (CO
2
) as the carbon source, hydrosilanes as reductants and
N
-heterocyclic carbenes (NHCs) as catalysts. Using CO
2
as a reagent has the advantage of low cost and negligible toxicity. However, the catalyst is air-sensitive and must be generated fresh before use; consequently, the techniques used to prepare and manipulate the catalyst are described. The synthetic approach described in this protocol does not use any toxic reagents; using the appropriate catalyst,
N
-formylated or
N
-methylated products can be obtained with high selectivity. The overall time for catalyst preparation and for conducting several catalytic reactions in parallel is 15–48 h, depending on the nature of the substrates.</description><subject>639/638/403/933</subject><subject>639/638/77/889</subject><subject>Amines</subject><subject>Analytical Chemistry</subject><subject>Biological Techniques</subject><subject>Carbenes</subject><subject>Carbon dioxide</subject><subject>Carbon sources</subject><subject>Catalysis</subject><subject>Catalysts</subject><subject>Computational Biology/Bioinformatics</subject><subject>Intermediates</subject><subject>Life Sciences</subject><subject>Ligands</subject><subject>Methods</subject><subject>Methylation</subject><subject>Microarrays</subject><subject>Organic Chemistry</subject><subject>Precious metals</subject><subject>Properties</subject><subject>Protocol</subject><subject>Reagents</subject><subject>Reducing agents</subject><subject>Selectivity</subject><subject>Substrates</subject><subject>Toxicity</subject><issn>1754-2189</issn><issn>1750-2799</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>BENPR</sourceid><recordid>eNp9ktFLHDEQxhdpQWv72ucFn6TsmWSz2c3jcWgryAlV8TFks5MzsptokgPvv-94WtqDawlkwszvmwkfUxRfKZlRUndn_imGPGOEihltm4PiCG9SsVbKD9s3rxjt5GHxKaVHQnhbi_aoyMvKhjhtRp1d8KX2Q7msJsgPvzPBlnpyHlK5Ts6vSqzpsbIRAMEHyBCD2ZjRmdLo2IMHjEhsUk7bbotrVuq0LWK3FNbRwOfio9Vjgi_v8bi4uzi_Xfyorq6_Xy7mV5VpCM0V1wIklwPhNYehofXAbW862jec9KQlhDLZm4ELSgUlUjBiekt52zOimRV1fVycvPVFZ57XkLJ6xPkeRyrWCC4k-iH_R9FONIxyLsgfaqVHUM7bkKM2k0tGzXmHpjdd0yE120PhGWByJniwDvM7gtMdATIZXvJKr1NSlzc_d9lv_2bnt_eL5d6vmBhSimDVU3STjhtFiXpdGLVdGPW6MArXAwVnb4KEoF9B_MuH_YpfYVDABQ</recordid><startdate>20170201</startdate><enddate>20170201</enddate><creator>Bobbink, Felix D</creator><creator>Das, Shoubhik</creator><creator>Dyson, Paul J</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>AAYXX</scope><scope>CITATION</scope><scope>ATWCN</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7T5</scope><scope>7T7</scope><scope>7TM</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>P64</scope><scope>PATMY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PYCSY</scope><scope>RC3</scope></search><sort><creationdate>20170201</creationdate><title>N-formylation and N-methylation of amines using metal-free N-heterocyclic carbene catalysts and CO2 as carbon source</title><author>Bobbink, Felix D ; Das, Shoubhik ; Dyson, Paul J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c501t-4a6e949d0434ed513d4fbc81b540b0700129bcd46116109620cbf147b20a2f633</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>639/638/403/933</topic><topic>639/638/77/889</topic><topic>Amines</topic><topic>Analytical Chemistry</topic><topic>Biological Techniques</topic><topic>Carbenes</topic><topic>Carbon dioxide</topic><topic>Carbon sources</topic><topic>Catalysis</topic><topic>Catalysts</topic><topic>Computational Biology/Bioinformatics</topic><topic>Intermediates</topic><topic>Life Sciences</topic><topic>Ligands</topic><topic>Methods</topic><topic>Methylation</topic><topic>Microarrays</topic><topic>Organic Chemistry</topic><topic>Precious metals</topic><topic>Properties</topic><topic>Protocol</topic><topic>Reagents</topic><topic>Reducing agents</topic><topic>Selectivity</topic><topic>Substrates</topic><topic>Toxicity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bobbink, Felix D</creatorcontrib><creatorcontrib>Das, Shoubhik</creatorcontrib><creatorcontrib>Dyson, Paul J</creatorcontrib><collection>CrossRef</collection><collection>Gale In Context: Middle School</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Immunology Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Nucleic Acids Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environmental Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Environmental Science Collection</collection><collection>Genetics Abstracts</collection><jtitle>Nature protocols</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bobbink, Felix D</au><au>Das, Shoubhik</au><au>Dyson, Paul J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>N-formylation and N-methylation of amines using metal-free N-heterocyclic carbene catalysts and CO2 as carbon source</atitle><jtitle>Nature protocols</jtitle><stitle>Nat Protoc</stitle><date>2017-02-01</date><risdate>2017</risdate><volume>12</volume><issue>2</issue><spage>417</spage><epage>428</epage><pages>417-428</pages><issn>1754-2189</issn><eissn>1750-2799</eissn><abstract>This protocol describes the environmentally benign
N
-formylation and
N
-methylation of primary and secondary amines using carbon dioxide as the carbon source, hydrosilanes as reductants and
N
-heterocyclic carbenes as catalysts.
N
-formylation and
N
-methylation of amines are important reactions that are used to produce a wide range of key intermediates and compounds. This protocol describes the environmentally benign
N
-formylation and
N
-methylation of primary and secondary amines using carbon dioxide (CO
2
) as the carbon source, hydrosilanes as reductants and
N
-heterocyclic carbenes (NHCs) as catalysts. Using CO
2
as a reagent has the advantage of low cost and negligible toxicity. However, the catalyst is air-sensitive and must be generated fresh before use; consequently, the techniques used to prepare and manipulate the catalyst are described. The synthetic approach described in this protocol does not use any toxic reagents; using the appropriate catalyst,
N
-formylated or
N
-methylated products can be obtained with high selectivity. The overall time for catalyst preparation and for conducting several catalytic reactions in parallel is 15–48 h, depending on the nature of the substrates.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><doi>10.1038/nprot.2016.175</doi><tpages>12</tpages></addata></record> |
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source | SpringerLink Journals; Nature |
subjects | 639/638/403/933 639/638/77/889 Amines Analytical Chemistry Biological Techniques Carbenes Carbon dioxide Carbon sources Catalysis Catalysts Computational Biology/Bioinformatics Intermediates Life Sciences Ligands Methods Methylation Microarrays Organic Chemistry Precious metals Properties Protocol Reagents Reducing agents Selectivity Substrates Toxicity |
title | N-formylation and N-methylation of amines using metal-free N-heterocyclic carbene catalysts and CO2 as carbon source |
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