N-Alkylation of amines with alcohols over nanosized zeolite beta

Direct N-alkylation of amines with alcohols was successfully performed by using nanosized zeolite beta, which showed the highest catalytic activity among other conventional zeolites. This method has several advantages, such as eco-friendliness, moderate to high yields, and simple work-up procedure....

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Green chemistry : an international journal and green chemistry resource : GC 2013-01, Vol.15 (12), p.3474-3483
Hauptverfasser: MARRI MAHENDER REDDY, MACHARLA ARUN KUMAR, SWAMY, Peraka, NARESH, Mameda, SRUJANA, Kodumuri, SATYANARAYANA, Lanka, VENUGOPAL, Akula, NARENDER, Nama
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 3483
container_issue 12
container_start_page 3474
container_title Green chemistry : an international journal and green chemistry resource : GC
container_volume 15
creator MARRI MAHENDER REDDY
MACHARLA ARUN KUMAR
SWAMY, Peraka
NARESH, Mameda
SRUJANA, Kodumuri
SATYANARAYANA, Lanka
VENUGOPAL, Akula
NARENDER, Nama
description Direct N-alkylation of amines with alcohols was successfully performed by using nanosized zeolite beta, which showed the highest catalytic activity among other conventional zeolites. This method has several advantages, such as eco-friendliness, moderate to high yields, and simple work-up procedure. The catalyst was successfully recovered and reused without significant loss of activity and only water is produced as co-product. In addition, imines were also efficiently prepared from the tandem reactions of amines with 2-, 3- and 4-nitrobenzyl alcohols using nanosized zeolite beta.
doi_str_mv 10.1039/c3gc41345d
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1492623129</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1492623129</sourcerecordid><originalsourceid>FETCH-LOGICAL-c294t-dde87236689bc1c3819d6651d702fe946188c1bff9411dcfbdddd4c43e60cb893</originalsourceid><addsrcrecordid>eNpFkE9LAzEUxIMoWKsXP0EuggireZs0u7lZxH9Q9KLnJZu82Gi6qclWaT-9LS31XeYdfjMwQ8g5sGtgXN0Y_mEEcDGyB2QAQvJClRU73P-yPCYnOX8yBlBJMSC3L8U4fC2D7n3saHRUz3yHmf76fkp1MHEaQ6bxBxPtdBezX6GlK4zB90hb7PUpOXI6ZDzb6ZC8P9y_3T0Vk9fH57vxpDClEn1hLdZVyaWsVWvA8BqUlXIEtmKlQyUk1LWB1jklAKxxrV2fMIKjZKatFR-Sy23uPMXvBea-mflsMATdYVzkBsSmHYdyg15tUZNizgldM09-ptOyAdZsZmr-Z1rDF7tcnY0OLunO-Lx3lJWqFJOc_wHoi2e3</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1492623129</pqid></control><display><type>article</type><title>N-Alkylation of amines with alcohols over nanosized zeolite beta</title><source>Royal Society Of Chemistry Journals 2008-</source><source>Alma/SFX Local Collection</source><creator>MARRI MAHENDER REDDY ; MACHARLA ARUN KUMAR ; SWAMY, Peraka ; NARESH, Mameda ; SRUJANA, Kodumuri ; SATYANARAYANA, Lanka ; VENUGOPAL, Akula ; NARENDER, Nama</creator><creatorcontrib>MARRI MAHENDER REDDY ; MACHARLA ARUN KUMAR ; SWAMY, Peraka ; NARESH, Mameda ; SRUJANA, Kodumuri ; SATYANARAYANA, Lanka ; VENUGOPAL, Akula ; NARENDER, Nama</creatorcontrib><description>Direct N-alkylation of amines with alcohols was successfully performed by using nanosized zeolite beta, which showed the highest catalytic activity among other conventional zeolites. This method has several advantages, such as eco-friendliness, moderate to high yields, and simple work-up procedure. The catalyst was successfully recovered and reused without significant loss of activity and only water is produced as co-product. In addition, imines were also efficiently prepared from the tandem reactions of amines with 2-, 3- and 4-nitrobenzyl alcohols using nanosized zeolite beta.</description><identifier>ISSN: 1463-9262</identifier><identifier>EISSN: 1463-9270</identifier><identifier>DOI: 10.1039/c3gc41345d</identifier><language>eng</language><publisher>Cambridge: Royal Society of Chemistry</publisher><subject>Alcohols ; Amines ; Beta ; Catalysis ; Catalysts: preparations and properties ; Chemistry ; Exact sciences and technology ; General and physical chemistry ; Imines ; Nanocomposites ; Nanomaterials ; Nanostructure ; Noncondensed benzenic compounds ; Organic chemistry ; Preparations and properties ; Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry ; Zeolites</subject><ispartof>Green chemistry : an international journal and green chemistry resource : GC, 2013-01, Vol.15 (12), p.3474-3483</ispartof><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c294t-dde87236689bc1c3819d6651d702fe946188c1bff9411dcfbdddd4c43e60cb893</citedby><cites>FETCH-LOGICAL-c294t-dde87236689bc1c3819d6651d702fe946188c1bff9411dcfbdddd4c43e60cb893</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=27979063$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>MARRI MAHENDER REDDY</creatorcontrib><creatorcontrib>MACHARLA ARUN KUMAR</creatorcontrib><creatorcontrib>SWAMY, Peraka</creatorcontrib><creatorcontrib>NARESH, Mameda</creatorcontrib><creatorcontrib>SRUJANA, Kodumuri</creatorcontrib><creatorcontrib>SATYANARAYANA, Lanka</creatorcontrib><creatorcontrib>VENUGOPAL, Akula</creatorcontrib><creatorcontrib>NARENDER, Nama</creatorcontrib><title>N-Alkylation of amines with alcohols over nanosized zeolite beta</title><title>Green chemistry : an international journal and green chemistry resource : GC</title><description>Direct N-alkylation of amines with alcohols was successfully performed by using nanosized zeolite beta, which showed the highest catalytic activity among other conventional zeolites. This method has several advantages, such as eco-friendliness, moderate to high yields, and simple work-up procedure. The catalyst was successfully recovered and reused without significant loss of activity and only water is produced as co-product. In addition, imines were also efficiently prepared from the tandem reactions of amines with 2-, 3- and 4-nitrobenzyl alcohols using nanosized zeolite beta.</description><subject>Alcohols</subject><subject>Amines</subject><subject>Beta</subject><subject>Catalysis</subject><subject>Catalysts: preparations and properties</subject><subject>Chemistry</subject><subject>Exact sciences and technology</subject><subject>General and physical chemistry</subject><subject>Imines</subject><subject>Nanocomposites</subject><subject>Nanomaterials</subject><subject>Nanostructure</subject><subject>Noncondensed benzenic compounds</subject><subject>Organic chemistry</subject><subject>Preparations and properties</subject><subject>Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry</subject><subject>Zeolites</subject><issn>1463-9262</issn><issn>1463-9270</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNpFkE9LAzEUxIMoWKsXP0EuggireZs0u7lZxH9Q9KLnJZu82Gi6qclWaT-9LS31XeYdfjMwQ8g5sGtgXN0Y_mEEcDGyB2QAQvJClRU73P-yPCYnOX8yBlBJMSC3L8U4fC2D7n3saHRUz3yHmf76fkp1MHEaQ6bxBxPtdBezX6GlK4zB90hb7PUpOXI6ZDzb6ZC8P9y_3T0Vk9fH57vxpDClEn1hLdZVyaWsVWvA8BqUlXIEtmKlQyUk1LWB1jklAKxxrV2fMIKjZKatFR-Sy23uPMXvBea-mflsMATdYVzkBsSmHYdyg15tUZNizgldM09-ptOyAdZsZmr-Z1rDF7tcnY0OLunO-Lx3lJWqFJOc_wHoi2e3</recordid><startdate>20130101</startdate><enddate>20130101</enddate><creator>MARRI MAHENDER REDDY</creator><creator>MACHARLA ARUN KUMAR</creator><creator>SWAMY, Peraka</creator><creator>NARESH, Mameda</creator><creator>SRUJANA, Kodumuri</creator><creator>SATYANARAYANA, Lanka</creator><creator>VENUGOPAL, Akula</creator><creator>NARENDER, Nama</creator><general>Royal Society of Chemistry</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope></search><sort><creationdate>20130101</creationdate><title>N-Alkylation of amines with alcohols over nanosized zeolite beta</title><author>MARRI MAHENDER REDDY ; MACHARLA ARUN KUMAR ; SWAMY, Peraka ; NARESH, Mameda ; SRUJANA, Kodumuri ; SATYANARAYANA, Lanka ; VENUGOPAL, Akula ; NARENDER, Nama</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c294t-dde87236689bc1c3819d6651d702fe946188c1bff9411dcfbdddd4c43e60cb893</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Alcohols</topic><topic>Amines</topic><topic>Beta</topic><topic>Catalysis</topic><topic>Catalysts: preparations and properties</topic><topic>Chemistry</topic><topic>Exact sciences and technology</topic><topic>General and physical chemistry</topic><topic>Imines</topic><topic>Nanocomposites</topic><topic>Nanomaterials</topic><topic>Nanostructure</topic><topic>Noncondensed benzenic compounds</topic><topic>Organic chemistry</topic><topic>Preparations and properties</topic><topic>Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry</topic><topic>Zeolites</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>MARRI MAHENDER REDDY</creatorcontrib><creatorcontrib>MACHARLA ARUN KUMAR</creatorcontrib><creatorcontrib>SWAMY, Peraka</creatorcontrib><creatorcontrib>NARESH, Mameda</creatorcontrib><creatorcontrib>SRUJANA, Kodumuri</creatorcontrib><creatorcontrib>SATYANARAYANA, Lanka</creatorcontrib><creatorcontrib>VENUGOPAL, Akula</creatorcontrib><creatorcontrib>NARENDER, Nama</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><jtitle>Green chemistry : an international journal and green chemistry resource : GC</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>MARRI MAHENDER REDDY</au><au>MACHARLA ARUN KUMAR</au><au>SWAMY, Peraka</au><au>NARESH, Mameda</au><au>SRUJANA, Kodumuri</au><au>SATYANARAYANA, Lanka</au><au>VENUGOPAL, Akula</au><au>NARENDER, Nama</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>N-Alkylation of amines with alcohols over nanosized zeolite beta</atitle><jtitle>Green chemistry : an international journal and green chemistry resource : GC</jtitle><date>2013-01-01</date><risdate>2013</risdate><volume>15</volume><issue>12</issue><spage>3474</spage><epage>3483</epage><pages>3474-3483</pages><issn>1463-9262</issn><eissn>1463-9270</eissn><abstract>Direct N-alkylation of amines with alcohols was successfully performed by using nanosized zeolite beta, which showed the highest catalytic activity among other conventional zeolites. This method has several advantages, such as eco-friendliness, moderate to high yields, and simple work-up procedure. The catalyst was successfully recovered and reused without significant loss of activity and only water is produced as co-product. In addition, imines were also efficiently prepared from the tandem reactions of amines with 2-, 3- and 4-nitrobenzyl alcohols using nanosized zeolite beta.</abstract><cop>Cambridge</cop><pub>Royal Society of Chemistry</pub><doi>10.1039/c3gc41345d</doi><tpages>10</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1463-9262
ispartof Green chemistry : an international journal and green chemistry resource : GC, 2013-01, Vol.15 (12), p.3474-3483
issn 1463-9262
1463-9270
language eng
recordid cdi_proquest_miscellaneous_1492623129
source Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection
subjects Alcohols
Amines
Beta
Catalysis
Catalysts: preparations and properties
Chemistry
Exact sciences and technology
General and physical chemistry
Imines
Nanocomposites
Nanomaterials
Nanostructure
Noncondensed benzenic compounds
Organic chemistry
Preparations and properties
Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry
Zeolites
title N-Alkylation of amines with alcohols over nanosized zeolite beta
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-01T01%3A52%3A35IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=N-Alkylation%20of%20amines%20with%20alcohols%20over%20nanosized%20zeolite%20beta&rft.jtitle=Green%20chemistry%20:%20an%20international%20journal%20and%20green%20chemistry%20resource%20:%20GC&rft.au=MARRI%20MAHENDER%20REDDY&rft.date=2013-01-01&rft.volume=15&rft.issue=12&rft.spage=3474&rft.epage=3483&rft.pages=3474-3483&rft.issn=1463-9262&rft.eissn=1463-9270&rft_id=info:doi/10.1039/c3gc41345d&rft_dat=%3Cproquest_cross%3E1492623129%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1492623129&rft_id=info:pmid/&rfr_iscdi=true