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<article article-type="research-article" dtd-version="1.3" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xml:lang="ru"><front><journal-meta><journal-id journal-id-type="publisher-id">vestich</journal-id><journal-title-group><journal-title xml:lang="ru">Известия Национальной академии наук Беларуси. Серия химических наук</journal-title><trans-title-group xml:lang="en"><trans-title>Proceedings of the National Academy of Sciences of Belarus, Chemical Series</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1561-8331</issn><issn pub-type="epub">2524-2342</issn><publisher><publisher-name>The Republican Unitary Enterprise Publishing House "Belaruskaya Navuka"</publisher-name></publisher></journal-meta><article-meta><article-id custom-type="elpub" pub-id-type="custom">vestich-72</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>ОРГАНИЧЕСКАЯ ХИМИЯ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>ORGANIC CHEMISTRY</subject></subj-group></article-categories><title-group><article-title>3,4,4,-Трихлорбут-3-еннитрил в синтезе полифункциональных соединений</article-title><trans-title-group xml:lang="en"><trans-title>3,4,4-Trichlorobut-3-enenitrile in synthesis of polyfunctional compounds</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Петкевич</surname><given-names>С. К.</given-names></name><name name-style="western" xml:lang="en"><surname>Petkevich</surname><given-names>S. K.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Клецков</surname><given-names>А. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Kletskov</surname><given-names>A. V.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Дикусар</surname><given-names>Е. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Dikusar</surname><given-names>E. A.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Зверева</surname><given-names>Т. Д.</given-names></name><name name-style="western" xml:lang="en"><surname>Zvereva</surname><given-names>T. D.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Жуковская</surname><given-names>Н. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Zhukovskaya</surname><given-names>N. A.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Розенцвейг</surname><given-names>И. Б.</given-names></name><name name-style="western" xml:lang="en"><surname>Rozentsveig</surname><given-names>I. B.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Левковская</surname><given-names>Г. Г.</given-names></name><name name-style="western" xml:lang="en"><surname>Levkovskaya</surname><given-names>G. G.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Поткин</surname><given-names>В. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Potkin</surname><given-names>V. I.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff xml:lang="ru" id="aff-1"><institution>Институт физико-органической химии НАН Беларуси</institution><country>Belarus</country></aff><aff xml:lang="ru" id="aff-2"><institution>Иркутский институт химии им. А. Е. Фаворского СО РАН</institution><country>Russian Federation</country></aff><pub-date pub-type="collection"><year>2014</year></pub-date><pub-date pub-type="epub"><day>08</day><month>06</month><year>2016</year></pub-date><volume>0</volume><issue>4</issue><fpage>44</fpage><lpage>50</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Петкевич С.К., Клецков А.В., Дикусар Е.А., Зверева Т.Д., Жуковская Н.А., Розенцвейг И.Б., Левковская Г.Г., Поткин В.И., 2016</copyright-statement><copyright-year>2016</copyright-year><copyright-holder xml:lang="ru">Петкевич С.К., Клецков А.В., Дикусар Е.А., Зверева Т.Д., Жуковская Н.А., Розенцвейг И.Б., Левковская Г.Г., Поткин В.И.</copyright-holder><copyright-holder xml:lang="en">Petkevich S.K., Kletskov A.V., Dikusar E.A., Zvereva T.D., Zhukovskaya N.A., Rozentsveig I.B., Levkovskaya G.G., Potkin V.I.</copyright-holder><license xml:lang="ru" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>Данная работа распространяется под лицензией Creative Commons Attribution 4.0.</license-p></license><license xml:lang="en" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>This work is licensed under a Creative Commons Attribution 4.0 License.</license-p></license></permissions><self-uri xlink:href="https://vestichem.belnauka.by/jour/article/view/72">https://vestichem.belnauka.by/jour/article/view/72</self-uri><abstract><p>Усовершенствован способ синтеза 3,4,4-трихлорбут-3-еннитрила на основе доступной 3,4,4-трихлорбут-3-еновой кислоты - продукта превращений трихлорэтилена. Получены продукты замещения интернального атома хлора в его молекуле на азидную группу, остаток моноэтаноламина, а также сложные эфиры последнего с 5-(п-толил)изоксазол- и 4,5-дихлоризотиазол-3-карбоновыми кислотами. При действии HCl протекало расщепление C-N связи в сложных эфирах с образованием гидрохлоридов аминоэфиров изоксазол- и изотиазол-3-карбоновых кислот, которые при ацилировании изоксазолил- и изотиазолилкарбонилхлоридами образовывали смешанные амидоэфиры с разными азольными остатками. Полученные соединения проходят биотестирование пестицидной активности и синергетического действия в композициях с инсектицидами.</p></abstract><trans-abstract xml:lang="en"><p>The method for synthesis of 3,4,4-trichlorobut-3-ennitrile has been improved. The substitution products of internal chlorine atom by azido group, monoethanolamine fragment and also its esters with 5-( p-tolyl)isoxazole- and 4,5-dichloroisothiazole-3-carboxylic acids have been prepared. It has been found that HCl cleaves C-N bond in esters producing hydrochlorides of isothiazole-3- and isoxazole-3-carboxylic acid aminoesters, which. Under acylation by isoxazolyl- and isothiazolyl carbonyl chlorides formed mixed amido esters with different azole moieties.</p></trans-abstract></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Кабердин Р. В., Поткин В. И. // Успехи химии. 1994. Т. 63, № 8. С. 673-693.</mixed-citation><mixed-citation xml:lang="en">Кабердин Р. В., Поткин В. И. // Успехи химии. 1994. Т. 63, № 8. С. 673-693.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Roedig A., Ritschel W. // Lieb. Ann. 1983. N 1. S. 18-23.</mixed-citation><mixed-citation xml:lang="en">Roedig A., Ritschel W. // Lieb. Ann. 1983. N 1. 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