Bromination of Acetanilide
A general procedure for bromination of aromatic compounds activated with electron donating substituents such as acetamido, hydroxyl, or ether groups is described. Bromine is generated in situ from potassium bromate and hydrobromic acid. This procedure avoids the hazards associated with direct handli...
Gespeichert in:
| Veröffentlicht in: | Journal of chemical education 1996-03, Vol.73 (3), p.267 |
|---|---|
| 1. Verfasser: | |
| Format: | Artikel |
| Sprache: | eng |
| Schlagworte: | |
| Online-Zugang: | Volltext |
| Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
| container_end_page | |
|---|---|
| container_issue | 3 |
| container_start_page | 267 |
| container_title | Journal of chemical education |
| container_volume | 73 |
| creator | Schatz, Paul F |
| description | A general procedure for bromination of aromatic compounds activated with electron donating substituents such as acetamido, hydroxyl, or ether groups is described. Bromine is generated in situ from potassium bromate and hydrobromic acid. This procedure avoids the hazards associated with direct handling of bromine or bromine solutions. The results from seven aromatic ethers and anilides are reported. |
| doi_str_mv | 10.1021/ed073p267 |
| format | Article |
| fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_211927476</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>9619658</sourcerecordid><originalsourceid>FETCH-LOGICAL-a216t-ae1a22bde44bc0b7f0e79ebd12e6e9039eda7da11359b972abfb14657fb0fcf03</originalsourceid><addsrcrecordid>eNplzzFPwzAQBWALgUQoDKxMFRIDQ-DOTuJ4LBW0SJVYYLbs-CylauNgpwP_nlRBMDDdcJ_e02PsGuEBgeMjOZCi55U8YRkqUecoeH3KMhifuSrr4pxdpLQFQF6qOmM3TzHs284Mbejmwc8XDQ2ma3eto0t25s0u0dXPnbGPl-f35TrfvK1el4tNbjhWQ24IDefWUVHYBqz0QFKRdcipIgVCkTPSGURRKqskN9ZbLKpSegu-8SBm7HbK7WP4PFAa9DYcYjdWao6ouCxkNaL7CTUxpBTJ6z62exO_NII-Lte_y0d7N1nTpL-s_-4bOvtWIg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>211927476</pqid></control><display><type>article</type><title>Bromination of Acetanilide</title><source>ACS Publications</source><creator>Schatz, Paul F</creator><creatorcontrib>Schatz, Paul F</creatorcontrib><description>A general procedure for bromination of aromatic compounds activated with electron donating substituents such as acetamido, hydroxyl, or ether groups is described. Bromine is generated in situ from potassium bromate and hydrobromic acid. This procedure avoids the hazards associated with direct handling of bromine or bromine solutions. The results from seven aromatic ethers and anilides are reported.</description><identifier>ISSN: 0021-9584</identifier><identifier>EISSN: 1938-1328</identifier><identifier>DOI: 10.1021/ed073p267</identifier><identifier>CODEN: JCEDA8</identifier><language>eng</language><publisher>Easton: Division of Chemical Education</publisher><subject>Acetanilide ; Aromatic compounds ; Bromination ; Bromine ; Bromine compounds ; Chemical reactions ; Experiments ; Ions ; Laboratories ; Organic chemistry ; Oxidation</subject><ispartof>Journal of chemical education, 1996-03, Vol.73 (3), p.267</ispartof><rights>Copyright American Chemical Society Mar 1996</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a216t-ae1a22bde44bc0b7f0e79ebd12e6e9039eda7da11359b972abfb14657fb0fcf03</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/ed073p267$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/ed073p267$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>315,782,786,2769,27085,27933,27934,56747,56797</link.rule.ids></links><search><creatorcontrib>Schatz, Paul F</creatorcontrib><title>Bromination of Acetanilide</title><title>Journal of chemical education</title><addtitle>J. Chem. Educ</addtitle><description>A general procedure for bromination of aromatic compounds activated with electron donating substituents such as acetamido, hydroxyl, or ether groups is described. Bromine is generated in situ from potassium bromate and hydrobromic acid. This procedure avoids the hazards associated with direct handling of bromine or bromine solutions. The results from seven aromatic ethers and anilides are reported.</description><subject>Acetanilide</subject><subject>Aromatic compounds</subject><subject>Bromination</subject><subject>Bromine</subject><subject>Bromine compounds</subject><subject>Chemical reactions</subject><subject>Experiments</subject><subject>Ions</subject><subject>Laboratories</subject><subject>Organic chemistry</subject><subject>Oxidation</subject><issn>0021-9584</issn><issn>1938-1328</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AIMQZ</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNplzzFPwzAQBWALgUQoDKxMFRIDQ-DOTuJ4LBW0SJVYYLbs-CylauNgpwP_nlRBMDDdcJ_e02PsGuEBgeMjOZCi55U8YRkqUecoeH3KMhifuSrr4pxdpLQFQF6qOmM3TzHs284Mbejmwc8XDQ2ma3eto0t25s0u0dXPnbGPl-f35TrfvK1el4tNbjhWQ24IDefWUVHYBqz0QFKRdcipIgVCkTPSGURRKqskN9ZbLKpSegu-8SBm7HbK7WP4PFAa9DYcYjdWao6ouCxkNaL7CTUxpBTJ6z62exO_NII-Lte_y0d7N1nTpL-s_-4bOvtWIg</recordid><startdate>199603</startdate><enddate>199603</enddate><creator>Schatz, Paul F</creator><general>Division of Chemical Education</general><general>American Chemical Society</general><scope>AAYXX</scope><scope>CITATION</scope><scope>0-V</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88B</scope><scope>88E</scope><scope>88I</scope><scope>8A4</scope><scope>8FE</scope><scope>8FG</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AIMQZ</scope><scope>ALSLI</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>BKSAR</scope><scope>CCPQU</scope><scope>CJNVE</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>LIQON</scope><scope>M0P</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M2P</scope><scope>MBDVC</scope><scope>PADUT</scope><scope>PCBAR</scope><scope>PDBOC</scope><scope>PQEDU</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope></search><sort><creationdate>199603</creationdate><title>Bromination of Acetanilide</title><author>Schatz, Paul F</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a216t-ae1a22bde44bc0b7f0e79ebd12e6e9039eda7da11359b972abfb14657fb0fcf03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>Acetanilide</topic><topic>Aromatic compounds</topic><topic>Bromination</topic><topic>Bromine</topic><topic>Bromine compounds</topic><topic>Chemical reactions</topic><topic>Experiments</topic><topic>Ions</topic><topic>Laboratories</topic><topic>Organic chemistry</topic><topic>Oxidation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Schatz, Paul F</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Social Sciences Premium Collection</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Education Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>Education Periodicals</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest One Literature</collection><collection>Social Science Premium Collection</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>Earth, Atmospheric & Aquatic Science Collection</collection><collection>ProQuest One Community College</collection><collection>Education Collection</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Materials Science Database</collection><collection>ProQuest One Literature - U.S. Customers Only</collection><collection>Education Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Science Database</collection><collection>Research Library (Corporate)</collection><collection>Research Library China</collection><collection>Earth, Atmospheric & Aquatic Science Database</collection><collection>Materials Science Collection</collection><collection>ProQuest One Education</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><jtitle>Journal of chemical education</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Schatz, Paul F</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Bromination of Acetanilide</atitle><jtitle>Journal of chemical education</jtitle><addtitle>J. Chem. Educ</addtitle><date>1996-03</date><risdate>1996</risdate><volume>73</volume><issue>3</issue><spage>267</spage><pages>267-</pages><issn>0021-9584</issn><eissn>1938-1328</eissn><coden>JCEDA8</coden><abstract>A general procedure for bromination of aromatic compounds activated with electron donating substituents such as acetamido, hydroxyl, or ether groups is described. Bromine is generated in situ from potassium bromate and hydrobromic acid. This procedure avoids the hazards associated with direct handling of bromine or bromine solutions. The results from seven aromatic ethers and anilides are reported.</abstract><cop>Easton</cop><pub>Division of Chemical Education</pub><doi>10.1021/ed073p267</doi></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 0021-9584 |
| ispartof | Journal of chemical education, 1996-03, Vol.73 (3), p.267 |
| issn | 0021-9584 1938-1328 |
| language | eng |
| recordid | cdi_proquest_journals_211927476 |
| source | ACS Publications |
| subjects | Acetanilide Aromatic compounds Bromination Bromine Bromine compounds Chemical reactions Experiments Ions Laboratories Organic chemistry Oxidation |
| title | Bromination of Acetanilide |
| url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-02T20%3A50%3A08IST&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=Bromination%20of%20Acetanilide&rft.jtitle=Journal%20of%20chemical%20education&rft.au=Schatz,%20Paul%20F&rft.date=1996-03&rft.volume=73&rft.issue=3&rft.spage=267&rft.pages=267-&rft.issn=0021-9584&rft.eissn=1938-1328&rft.coden=JCEDA8&rft_id=info:doi/10.1021/ed073p267&rft_dat=%3Cproquest_cross%3E9619658%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=211927476&rft_id=info:pmid/&rfr_iscdi=true |