Sciact
  • EN
  • RU

REARRANGEMENT OF THE CARBON SKELETON OF PERFLUORINATED 1-ISOPROPYLBENZOCYLOBUTENES 1-METHYL-1-ISOPROPYLBENZOCYLOBUTENES AND 1-METHYL-2-ISOPROPYLBENZOCYLOBUTENES BY THE ACTION OF ANTIMONY PENTAFLUORIDE Научная публикация

Журнал BULLETIN OF THE RUSSIAN ACADEMY OF SCIENCES-DIVISION OF CHEMICAL SCIENCE
ISSN: 1063-5211
Вых. Данные Год: 1992, Том: 41, Номер: 6, Страницы: 1110-1114 Страниц : 5 DOI: 10.1007/BF00866598
Ключевые слова PERFLUOROALKYLBENZOCYCLOBUTENES; PERFLUOROALKYLSTYRENES; PERFLUOROALKYLINDANS; ANTIMONY PENTAFLUORIDE; CATIONOID SKELETAL TRANSFORMATIONS
Авторы Karpov V.M. 1 , Mezhenkova T.V. 1 , Platonov V.E. 1
Организации
1 N.N. Vorozhtsov Novosibirsk Institute of Organic Chemistry of Siberian Branch of Russian Academy of Sciences

Реферат: Perfluorinated 1-isopropyl-, 1-methyl-1-isopropyl-, and 1-methyl-2-isopropylbenzocyclobutenes isomerize under the influence of antimony pentafluoride to perfluorinated alkylstyrenes and alkylindans. The process may be accompanied by dealkylation and also by fluorination and defluorination of the products. With antimony pentafluoride at 50-degrees-C perfluoro-1-methyl-1-isopropylbenzocyclobutene gives perfluoro-alpha,beta,beta,o-tetramethylstyrene, which isomerizes under the influence of antiniony pentafluoride at 130-degrees-C into perfluoro-1,2,2-trimethylindan, and the latter forms perfluoro-2,3-dimethylindene under the reaction conditions. Perfluoro-1-methyl-2-isopropylbenzocyclobutene is not changed in the presence of antimony pentafluoride at 50-degrees-C but isomerizes to perfluoro-1-isopropylindan at 90-degrees-C. The latter is transformed under these conditions into the above-mentioned tetramethylstyrene. Perfluoro-1-isopropylbenzocyclobutene does not react with antimony pentafluoride at 130-degrees-C, but at 170-degrees-C it gives a mixture of perfluorinated 2,2-dimethylindan, 2,3-dimethylindene, 2,3-dimethyl-4,5,6,7-tetrahydroindene, and 2-isobutyltoluene, which is converted into perfluoro-o-xylene under the reaction conditions.
Библиографическая ссылка: Karpov V.M. , Mezhenkova T.V. , Platonov V.E.
REARRANGEMENT OF THE CARBON SKELETON OF PERFLUORINATED 1-ISOPROPYLBENZOCYLOBUTENES 1-METHYL-1-ISOPROPYLBENZOCYLOBUTENES AND 1-METHYL-2-ISOPROPYLBENZOCYLOBUTENES BY THE ACTION OF ANTIMONY PENTAFLUORIDE
BULLETIN OF THE RUSSIAN ACADEMY OF SCIENCES-DIVISION OF CHEMICAL SCIENCE. 1992. V.41. N6. P.1110-1114. DOI: 10.1007/BF00866598 WOS Scopus РИНЦ OpenAlex
Даты:
Опубликована в печати: 1 июн. 1992 г.
Идентификаторы БД:
Web of science: WOS:A1992KU70200013
Scopus: 2-s2.0-34249834188
РИНЦ: 31340178
OpenAlex: W1998792996
Цитирование в БД:
БД Цитирований
Web of science 7
Scopus 8
OpenAlex 8
Альметрики: