Acetylation of aromatic ethers using acetic anhydride over solid acid catalysts in a solvent-free system. Scope of the reaction for substituted ethers

The acetylation of aryl ethers using acetic anhydride in the presence of zeolites under modest conditions in a solvent-free system gave the corresponding para-acetylated products in high yields. The zeolite can be recovered, regenerated and reused to give almost the same yield as that given when fre...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Organic & biomolecular chemistry 2003-05, Vol.1 (9), p.1560-1564
Hauptverfasser: Smith, Keith, el-Hiti, Gamal A, Jayne, Anthony J, Butters, Michael
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1564
container_issue 9
container_start_page 1560
container_title Organic & biomolecular chemistry
container_volume 1
creator Smith, Keith
el-Hiti, Gamal A
Jayne, Anthony J
Butters, Michael
description The acetylation of aryl ethers using acetic anhydride in the presence of zeolites under modest conditions in a solvent-free system gave the corresponding para-acetylated products in high yields. The zeolite can be recovered, regenerated and reused to give almost the same yield as that given when fresh zeolite is used.
doi_str_mv 10.1039/b301260c
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_73587621</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>73587621</sourcerecordid><originalsourceid>FETCH-LOGICAL-c399t-87d618ccb2f4a74d40a7b65c8a0a7fb375ccc0bb46c3380c9e93379e303284fe3</originalsourceid><addsrcrecordid>eNpFkV1LwzAUhoMobk7BXyC5Em86k6Ztmssx_IKBF-p1SU9PXaVtZpIO-kf8vWZu6s35fHhfOIeQS87mnAl1WwrG44zBEZnyRMqIpUId_9Uxm5Az5z4Y40pmySmZ8FjFWZzLKflaAPqx1b4xPTU11dZ0oQGKfo3W0cE1_TvVAQoz3a_HyjYVUrNFS51pmyrsQgDtdTs672jTU73bbLH3UW0RqQtz7Ob0BcwGdx5BmVrU8ONZmyA0lM43fvBYHXzPyUmtW4cXhzwjb_d3r8vHaPX88LRcrCIQSvkol1XGc4AyrhMtkyphWpZZCrkORV0KmQIAK8skAyFyBgqVEFKhYCLOkxrFjFzvdTfWfA7ofNE1DrBtdY9mcIUUaS6zmAfwZg-CNc5ZrIuNbTptx4KzYveD4vcHAb06aA5lh9U_eDi6-AaPyoSo</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>73587621</pqid></control><display><type>article</type><title>Acetylation of aromatic ethers using acetic anhydride over solid acid catalysts in a solvent-free system. Scope of the reaction for substituted ethers</title><source>Royal Society Of Chemistry Journals</source><source>Royal Society of Chemistry Journals Archive (1841-2007)</source><source>Alma/SFX Local Collection</source><creator>Smith, Keith ; el-Hiti, Gamal A ; Jayne, Anthony J ; Butters, Michael</creator><creatorcontrib>Smith, Keith ; el-Hiti, Gamal A ; Jayne, Anthony J ; Butters, Michael</creatorcontrib><description>The acetylation of aryl ethers using acetic anhydride in the presence of zeolites under modest conditions in a solvent-free system gave the corresponding para-acetylated products in high yields. The zeolite can be recovered, regenerated and reused to give almost the same yield as that given when fresh zeolite is used.</description><identifier>ISSN: 1477-0520</identifier><identifier>EISSN: 1477-0539</identifier><identifier>DOI: 10.1039/b301260c</identifier><identifier>PMID: 12926287</identifier><language>eng</language><publisher>England</publisher><ispartof>Organic &amp; biomolecular chemistry, 2003-05, Vol.1 (9), p.1560-1564</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c399t-87d618ccb2f4a74d40a7b65c8a0a7fb375ccc0bb46c3380c9e93379e303284fe3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,2831,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12926287$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Smith, Keith</creatorcontrib><creatorcontrib>el-Hiti, Gamal A</creatorcontrib><creatorcontrib>Jayne, Anthony J</creatorcontrib><creatorcontrib>Butters, Michael</creatorcontrib><title>Acetylation of aromatic ethers using acetic anhydride over solid acid catalysts in a solvent-free system. Scope of the reaction for substituted ethers</title><title>Organic &amp; biomolecular chemistry</title><addtitle>Org Biomol Chem</addtitle><description>The acetylation of aryl ethers using acetic anhydride in the presence of zeolites under modest conditions in a solvent-free system gave the corresponding para-acetylated products in high yields. The zeolite can be recovered, regenerated and reused to give almost the same yield as that given when fresh zeolite is used.</description><issn>1477-0520</issn><issn>1477-0539</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><recordid>eNpFkV1LwzAUhoMobk7BXyC5Em86k6Ztmssx_IKBF-p1SU9PXaVtZpIO-kf8vWZu6s35fHhfOIeQS87mnAl1WwrG44zBEZnyRMqIpUId_9Uxm5Az5z4Y40pmySmZ8FjFWZzLKflaAPqx1b4xPTU11dZ0oQGKfo3W0cE1_TvVAQoz3a_HyjYVUrNFS51pmyrsQgDtdTs672jTU73bbLH3UW0RqQtz7Ob0BcwGdx5BmVrU8ONZmyA0lM43fvBYHXzPyUmtW4cXhzwjb_d3r8vHaPX88LRcrCIQSvkol1XGc4AyrhMtkyphWpZZCrkORV0KmQIAK8skAyFyBgqVEFKhYCLOkxrFjFzvdTfWfA7ofNE1DrBtdY9mcIUUaS6zmAfwZg-CNc5ZrIuNbTptx4KzYveD4vcHAb06aA5lh9U_eDi6-AaPyoSo</recordid><startdate>20030507</startdate><enddate>20030507</enddate><creator>Smith, Keith</creator><creator>el-Hiti, Gamal A</creator><creator>Jayne, Anthony J</creator><creator>Butters, Michael</creator><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20030507</creationdate><title>Acetylation of aromatic ethers using acetic anhydride over solid acid catalysts in a solvent-free system. Scope of the reaction for substituted ethers</title><author>Smith, Keith ; el-Hiti, Gamal A ; Jayne, Anthony J ; Butters, Michael</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c399t-87d618ccb2f4a74d40a7b65c8a0a7fb375ccc0bb46c3380c9e93379e303284fe3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Smith, Keith</creatorcontrib><creatorcontrib>el-Hiti, Gamal A</creatorcontrib><creatorcontrib>Jayne, Anthony J</creatorcontrib><creatorcontrib>Butters, Michael</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Organic &amp; biomolecular chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Smith, Keith</au><au>el-Hiti, Gamal A</au><au>Jayne, Anthony J</au><au>Butters, Michael</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Acetylation of aromatic ethers using acetic anhydride over solid acid catalysts in a solvent-free system. Scope of the reaction for substituted ethers</atitle><jtitle>Organic &amp; biomolecular chemistry</jtitle><addtitle>Org Biomol Chem</addtitle><date>2003-05-07</date><risdate>2003</risdate><volume>1</volume><issue>9</issue><spage>1560</spage><epage>1564</epage><pages>1560-1564</pages><issn>1477-0520</issn><eissn>1477-0539</eissn><abstract>The acetylation of aryl ethers using acetic anhydride in the presence of zeolites under modest conditions in a solvent-free system gave the corresponding para-acetylated products in high yields. The zeolite can be recovered, regenerated and reused to give almost the same yield as that given when fresh zeolite is used.</abstract><cop>England</cop><pmid>12926287</pmid><doi>10.1039/b301260c</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1477-0520
ispartof Organic & biomolecular chemistry, 2003-05, Vol.1 (9), p.1560-1564
issn 1477-0520
1477-0539
language eng
recordid cdi_proquest_miscellaneous_73587621
source Royal Society Of Chemistry Journals; Royal Society of Chemistry Journals Archive (1841-2007); Alma/SFX Local Collection
title Acetylation of aromatic ethers using acetic anhydride over solid acid catalysts in a solvent-free system. Scope of the reaction for substituted ethers
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-22T09%3A12%3A12IST&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=Acetylation%20of%20aromatic%20ethers%20using%20acetic%20anhydride%20over%20solid%20acid%20catalysts%20in%20a%20solvent-free%20system.%20Scope%20of%20the%20reaction%20for%20substituted%20ethers&rft.jtitle=Organic%20&%20biomolecular%20chemistry&rft.au=Smith,%20Keith&rft.date=2003-05-07&rft.volume=1&rft.issue=9&rft.spage=1560&rft.epage=1564&rft.pages=1560-1564&rft.issn=1477-0520&rft.eissn=1477-0539&rft_id=info:doi/10.1039/b301260c&rft_dat=%3Cproquest_cross%3E73587621%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=73587621&rft_id=info:pmid/12926287&rfr_iscdi=true