Transformations of perfluorinated 1-alkyl-, 1-phenyl- and 1,2-dialkylbenzocyclobutenes under the action of SiO2/SbF5 Научная публикация
Журнал |
Journal of Fluorine Chemistry
ISSN: 0022-1139 |
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Вых. Данные | Год: 2013, Том: 145, Страницы: 41-50 Страниц : DOI: 10.1016/j.jfluchem.2012.11.004 | ||
Ключевые слова | Perfluorinated; Benzocyclobutenes; Phthalides; Phthalanes; Silicon dioxide; Antimony pentafluoride | ||
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Организации |
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Реферат:
Heating of perfluorinated 1-methyl-, 1-ethyl- and 1-isopropylbenzocyclobutenes with SiO2 in an SbF5 medium at 75 degrees C results in perfluoro-2-alkylbenzocyclobutenones or perfluoro-3-alkylphthalides formation. Perfluorinated 1,2-diethyl- and 1-ethyl-2-methylbenzocyclobutenes react with SiO2/SbF5 at 75 degrees C to form, after treatment of the reaction mixture with water, perfluorinated 1,3-diethyl- and 1-ethyl-3-methylphthalan-1,3-diol, respectively. Perfluoro-1,2-diisopropylbenzocyclobutene under the action of SiO2/SbF5 at 95 degrees C is converted to perfluoro-7,8-diisopropylbicyclo[4.2.0]octa-1,5,7-triene-3,4-dione and perfluoro-1,2-diisobutyrylbenzene. Perfluoro-1-methyl-2-phenylbenzocyclobutene does not react with SiO2 in an SbF5 medium at 75 degrees C, perfluoro-1-phenylbenzocyclobutene in analogous conditions gives a mixture of perfluorinated 2-hydroxy-2-phenylbenzocyclobutenone and 2-benzoylbenzoic acid. (c) 2012 Elsevier B.V. All rights reserved.
Библиографическая ссылка:
Zonov Y.V.
, Karpov V.M.
, Platonov V.E.
, Rybalova T.V.
Transformations of perfluorinated 1-alkyl-, 1-phenyl- and 1,2-dialkylbenzocyclobutenes under the action of SiO2/SbF5
Journal of Fluorine Chemistry. 2013. V.145. P.41-50. DOI: 10.1016/j.jfluchem.2012.11.004 WOS Scopus РИНЦ
Transformations of perfluorinated 1-alkyl-, 1-phenyl- and 1,2-dialkylbenzocyclobutenes under the action of SiO2/SbF5
Journal of Fluorine Chemistry. 2013. V.145. P.41-50. DOI: 10.1016/j.jfluchem.2012.11.004 WOS Scopus РИНЦ
Даты:
Опубликована в печати: | 1 янв. 2013 г. |
Идентификаторы:
Web of science | WOS:000315252900005 |
Scopus | 2-s2.0-84871903767 |
РИНЦ | 20416952 |
OpenAlex | W2050393366 |