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A new efficient route for the synthesis of 4,4′,6,6′-tetra(azido)azo-1,3,5-triazine
A new method for the synthesis of 4,4′,6,6′-tetra(azido)azo-1,3,5-triazine (TAAT) is described. The key intermediate 4,4′,6,6′-tetra(azido)hydrazo-1,3,5-triazine (TAHT) was synthesized by nucleophilic substitution in the case of sodium azide as nucleophile. N-Bromosuccinide (NBS) was used as oxidant...
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Published in: | Chinese chemical letters 2007-09, Vol.18 (9), p.1037-1039 |
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container_issue | 9 |
container_start_page | 1037 |
container_title | Chinese chemical letters |
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creator | Li, Xiao Tong Li, Sheng Hua Pang, Si Ping Yu, Yong Zhong Luo, Yun Jun |
description | A new method for the synthesis of 4,4′,6,6′-tetra(azido)azo-1,3,5-triazine (TAAT) is described. The key intermediate 4,4′,6,6′-tetra(azido)hydrazo-1,3,5-triazine (TAHT) was synthesized by nucleophilic substitution in the case of sodium azide as nucleophile.
N-Bromosuccinide (NBS) was used as oxidant to oxidize TAHT by a tractable operation under mild reaction condition. The target compound TAAT was obtained with a facile process and high overall yield of 81%. The structures of TAAT and its intermediates were identified by spectroscopic methods. |
doi_str_mv | 10.1016/j.cclet.2007.06.028 |
format | article |
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N-Bromosuccinide (NBS) was used as oxidant to oxidize TAHT by a tractable operation under mild reaction condition. The target compound TAAT was obtained with a facile process and high overall yield of 81%. The structures of TAAT and its intermediates were identified by spectroscopic methods.</description><identifier>ISSN: 1001-8417</identifier><identifier>EISSN: 1878-5964</identifier><identifier>DOI: 10.1016/j.cclet.2007.06.028</identifier><language>eng</language><publisher>Elsevier B.V</publisher><subject>Azide ; High-nitrogen compounds ; Synthesis ; Triazine</subject><ispartof>Chinese chemical letters, 2007-09, Vol.18 (9), p.1037-1039</ispartof><rights>2007 Si Ping Pang</rights><rights>Copyright © Wanfang Data Co. Ltd. All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c335t-3b5edd3fe9cecfde2b383c717ac0fb640c1f3470cb00078d051397f4b3b4be8f3</citedby><cites>FETCH-LOGICAL-c335t-3b5edd3fe9cecfde2b383c717ac0fb640c1f3470cb00078d051397f4b3b4be8f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.wanfangdata.com.cn/images/PeriodicalImages/zghxkb/zghxkb.jpg</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids></links><search><creatorcontrib>Li, Xiao Tong</creatorcontrib><creatorcontrib>Li, Sheng Hua</creatorcontrib><creatorcontrib>Pang, Si Ping</creatorcontrib><creatorcontrib>Yu, Yong Zhong</creatorcontrib><creatorcontrib>Luo, Yun Jun</creatorcontrib><title>A new efficient route for the synthesis of 4,4′,6,6′-tetra(azido)azo-1,3,5-triazine</title><title>Chinese chemical letters</title><description>A new method for the synthesis of 4,4′,6,6′-tetra(azido)azo-1,3,5-triazine (TAAT) is described. The key intermediate 4,4′,6,6′-tetra(azido)hydrazo-1,3,5-triazine (TAHT) was synthesized by nucleophilic substitution in the case of sodium azide as nucleophile.
N-Bromosuccinide (NBS) was used as oxidant to oxidize TAHT by a tractable operation under mild reaction condition. The target compound TAAT was obtained with a facile process and high overall yield of 81%. The structures of TAAT and its intermediates were identified by spectroscopic methods.</description><subject>Azide</subject><subject>High-nitrogen compounds</subject><subject>Synthesis</subject><subject>Triazine</subject><issn>1001-8417</issn><issn>1878-5964</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><recordid>eNp9kE1OwzAQhSMEEqVwAjbeAVISxnXipAsWVcWfVIkNiKUVO-PWoSTIdintijNxJE6CQ1mzeqPRezN6XxSdUkgpUH7ZpEot0acjgCIFnsKo3IsGtCzKJB_zbD_MADQpM1ocRkfONRAcJeOD6HlCWlwT1Noog60ntlt5JLqzxC-QuE0bxBlHOk2yOPv-_Ip5zIMkHr2tzqutqbuLatslNGZxnnhrwqrF4-hAV0uHJ386jJ5urh-nd8ns4fZ-OpklirHcJ0zmWNdM41ih0jWOJCuZKmhRKdCSZ6CoZlkBSkKoVtaQUzYudCaZzCSWmg2js93dddXqqp2LplvZNnwU2_ni40X2RGAMkAcn2zmV7ZyzqMWbNa-V3QgKoqcoGvFLUfQZAVwERiF1tUthKPFu0ArXc1JYG4vKi7oz_-Z_AHKvfNs</recordid><startdate>20070901</startdate><enddate>20070901</enddate><creator>Li, Xiao Tong</creator><creator>Li, Sheng Hua</creator><creator>Pang, Si Ping</creator><creator>Yu, Yong Zhong</creator><creator>Luo, Yun Jun</creator><general>Elsevier B.V</general><general>School of Materials Science & Engineering, Beijing Institute of Technology, Beijing 100081, China%School of Life Science & Technology, Beijing Institute of Technology, Beijing 100081, China</general><scope>AAYXX</scope><scope>CITATION</scope><scope>2B.</scope><scope>4A8</scope><scope>92I</scope><scope>93N</scope><scope>PSX</scope><scope>TCJ</scope></search><sort><creationdate>20070901</creationdate><title>A new efficient route for the synthesis of 4,4′,6,6′-tetra(azido)azo-1,3,5-triazine</title><author>Li, Xiao Tong ; Li, Sheng Hua ; Pang, Si Ping ; Yu, Yong Zhong ; Luo, Yun Jun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c335t-3b5edd3fe9cecfde2b383c717ac0fb640c1f3470cb00078d051397f4b3b4be8f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Azide</topic><topic>High-nitrogen compounds</topic><topic>Synthesis</topic><topic>Triazine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Xiao Tong</creatorcontrib><creatorcontrib>Li, Sheng Hua</creatorcontrib><creatorcontrib>Pang, Si Ping</creatorcontrib><creatorcontrib>Yu, Yong Zhong</creatorcontrib><creatorcontrib>Luo, Yun Jun</creatorcontrib><collection>CrossRef</collection><collection>Wanfang Data Journals - Hong Kong</collection><collection>WANFANG Data Centre</collection><collection>Wanfang Data Journals</collection><collection>万方数据期刊 - 香港版</collection><collection>China Online Journals (COJ)</collection><collection>China Online Journals (COJ)</collection><jtitle>Chinese chemical letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Xiao Tong</au><au>Li, Sheng Hua</au><au>Pang, Si Ping</au><au>Yu, Yong Zhong</au><au>Luo, Yun Jun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A new efficient route for the synthesis of 4,4′,6,6′-tetra(azido)azo-1,3,5-triazine</atitle><jtitle>Chinese chemical letters</jtitle><date>2007-09-01</date><risdate>2007</risdate><volume>18</volume><issue>9</issue><spage>1037</spage><epage>1039</epage><pages>1037-1039</pages><issn>1001-8417</issn><eissn>1878-5964</eissn><abstract>A new method for the synthesis of 4,4′,6,6′-tetra(azido)azo-1,3,5-triazine (TAAT) is described. The key intermediate 4,4′,6,6′-tetra(azido)hydrazo-1,3,5-triazine (TAHT) was synthesized by nucleophilic substitution in the case of sodium azide as nucleophile.
N-Bromosuccinide (NBS) was used as oxidant to oxidize TAHT by a tractable operation under mild reaction condition. The target compound TAAT was obtained with a facile process and high overall yield of 81%. The structures of TAAT and its intermediates were identified by spectroscopic methods.</abstract><pub>Elsevier B.V</pub><doi>10.1016/j.cclet.2007.06.028</doi><tpages>3</tpages></addata></record> |
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subjects | Azide High-nitrogen compounds Synthesis Triazine |
title | A new efficient route for the synthesis of 4,4′,6,6′-tetra(azido)azo-1,3,5-triazine |
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