High-yield nitration of benzene in the synthesis of 15N-labelled nitrobenzene, acetanilide, and diphenylamine
Labelled H15NO3 was used as the least‐cost source of nitrogen label to prepare nitrobenzene by reaction of acetyl nitrate with excess benzene. This labelled product was subsequently converted to acetanilide‐15N and diphenylamine‐15N.
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Veröffentlicht in: | Journal of labelled compounds & radiopharmaceuticals 1990-11, Vol.28 (11), p.1243-1245 |
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container_title | Journal of labelled compounds & radiopharmaceuticals |
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creator | Konior, Raymond J. Yang, Ling Walter, Robert I. |
description | Labelled H15NO3 was used as the least‐cost source of nitrogen label to prepare nitrobenzene by reaction of acetyl nitrate with excess benzene. This labelled product was subsequently converted to acetanilide‐15N and diphenylamine‐15N. |
doi_str_mv | 10.1002/jlcr.2580281103 |
format | Article |
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This labelled product was subsequently converted to acetanilide‐15N and diphenylamine‐15N.</description><subject>acetanilide-15N</subject><subject>acetyl nitrate</subject><subject>diphenylamine-15N</subject><subject>nitrobenzene-15N</subject><issn>0362-4803</issn><issn>1099-1344</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1990</creationdate><recordtype>article</recordtype><recordid>eNpFkFFLwzAUhYMoOKfPvuYHmJk0aZvgkwzdnGPiGPgY0ubGZWbZaAtaf70tG-7pcDjnu3APQreMjhilyf0mlNUoSSVNJGOUn6EBo0oRxoU4RwPKs4QISfkluqrrDaVdJsQAbaf-c01aD8Hi6JvKNH4X8c7hAuIvRMA-4mYNuG5jJ7Wv-4ylCxJMASHAgdod23fYlNCY6IO3vYkWW79fQ2yD2foI1-jCmVDDzVGHaPX8tBpPyfxt8jJ-nBOvKCdF94FQGQBTmSgSnqlEpkVphXKlyZxUubW5s1baggmXSseLUjrqEgrW0JLxIXo4nP32AVq9r_zWVK1mVPdL6X4pfVpKz-bj5cl2NDnQvm7g55821ZfOcp6n-mMx0ensfcmWr7lm_A_E-HEb</recordid><startdate>199011</startdate><enddate>199011</enddate><creator>Konior, Raymond J.</creator><creator>Yang, Ling</creator><creator>Walter, Robert I.</creator><general>John Wiley & Sons, Ltd</general><scope>BSCLL</scope></search><sort><creationdate>199011</creationdate><title>High-yield nitration of benzene in the synthesis of 15N-labelled nitrobenzene, acetanilide, and diphenylamine</title><author>Konior, Raymond J. ; Yang, Ling ; Walter, Robert I.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-i903-b281496ee1964b2369285bcd49fca6f897dd7fdd8db14f58f3bc8f0f20eda0c13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1990</creationdate><topic>acetanilide-15N</topic><topic>acetyl nitrate</topic><topic>diphenylamine-15N</topic><topic>nitrobenzene-15N</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Konior, Raymond J.</creatorcontrib><creatorcontrib>Yang, Ling</creatorcontrib><creatorcontrib>Walter, Robert I.</creatorcontrib><collection>Istex</collection><jtitle>Journal of labelled compounds & radiopharmaceuticals</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Konior, Raymond J.</au><au>Yang, Ling</au><au>Walter, Robert I.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>High-yield nitration of benzene in the synthesis of 15N-labelled nitrobenzene, acetanilide, and diphenylamine</atitle><jtitle>Journal of labelled compounds & radiopharmaceuticals</jtitle><addtitle>J Label Compd Radiopharm</addtitle><date>1990-11</date><risdate>1990</risdate><volume>28</volume><issue>11</issue><spage>1243</spage><epage>1245</epage><pages>1243-1245</pages><issn>0362-4803</issn><eissn>1099-1344</eissn><abstract>Labelled H15NO3 was used as the least‐cost source of nitrogen label to prepare nitrobenzene by reaction of acetyl nitrate with excess benzene. This labelled product was subsequently converted to acetanilide‐15N and diphenylamine‐15N.</abstract><cop>Chichester</cop><pub>John Wiley & Sons, Ltd</pub><doi>10.1002/jlcr.2580281103</doi><tpages>3</tpages></addata></record> |
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issn | 0362-4803 1099-1344 |
language | eng |
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source | Access via Wiley Online Library |
subjects | acetanilide-15N acetyl nitrate diphenylamine-15N nitrobenzene-15N |
title | High-yield nitration of benzene in the synthesis of 15N-labelled nitrobenzene, acetanilide, and diphenylamine |
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