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Synthesis of Potassium 4-(1-azol-1-yl)-2,3,5,6-tetrafluorophenyltrifluoroborates from K[C6F5BF3] and Alkali Metal Azol-1-ides. The Dramatic Distinction in Nucleophilicity of Alkali Metal Azol-1-ides and Dialkylamides Научная публикация

Журнал Journal of Fluorine Chemistry
ISSN: 0022-1139
Вых. Данные Год: 2013, Том: 156, Страницы: 290-297 Страниц : 8 DOI: 10.1016/j.jfluchem.2013.07.011
Ключевые слова N-nucleophile, NMR spectroscopy, Nucleophilic substitution, Pentafluorophenyltrifluoroborate
Авторы Shabalin A.Y. 1 , Adonin N.Y. 1 , Bardin V.V. 1,2 , Taran O.P. 1 , Ayusheev A.B. 1 , Parmon V.N. 1
Организации
1 G.K. Boreskov Institute of Catalysis, SB RAS, Acad. Lavrentjev Ave. 5, 630090 Novosibirsk, Russian Federation
2 N.N. Vorozhtsov Novosibirsk Institute of Organic Chemistry, SB RAS, Acad. Lavrentjev Ave. 9, 630090 Novosibirsk, Russian Federation

Информация о финансировании (1)

1 Министерство образования и науки Российской Федерации 2012-1.2.1-12-000-1004-038

Реферат: Nucleophilic substitution of fluorine atom in K[C6F5BF3] with alkali metal azol-1-ides in polar aprotic solvent (DMF, DMSO) at 60–130 °C gives potassium 4-(azol-1-yl)-2,3,5,6-tetrafluorophenyltrifluoroborates, K[4-AzC6F4BF3] (AzH = pyrrole, pyrazole, imidazole, indole, and benzimidazole). Unexpectedly, diethylamine and morpholine do not react with K[C6F5BF3] under the same conditions while pentafluorobenzene and R2NC6F4H form at 150 °C. Reaction of K[C6F5BF3] with Na[NR2] in diglyme or DMSO proceeds similar way. The assumed reason is the relatively low nucleophilicity of both secondary amines and alkali metal dialkylamides which results in destructive by-reaction with K[C6F5BF3] rather than in its aminodefluorination. This is confirmed by the competitive nucleophilic aminodefluorination of a model substrate, C6F5Ph, with sodium indolide/sodium morpholinide.
Библиографическая ссылка: Shabalin A.Y. , Adonin N.Y. , Bardin V.V. , Taran O.P. , Ayusheev A.B. , Parmon V.N.
Synthesis of Potassium 4-(1-azol-1-yl)-2,3,5,6-tetrafluorophenyltrifluoroborates from K[C6F5BF3] and Alkali Metal Azol-1-ides. The Dramatic Distinction in Nucleophilicity of Alkali Metal Azol-1-ides and Dialkylamides
Journal of Fluorine Chemistry. 2013. V.156. P.290-297. DOI: 10.1016/j.jfluchem.2013.07.011 WOS Scopus РИНЦ CAPlusCA OpenAlex
Даты:
Поступила в редакцию: 27 мая 2013 г.
Принята к публикации: 15 июл. 2013 г.
Опубликована online: 24 июл. 2013 г.
Опубликована в печати: 1 дек. 2013 г.
Идентификаторы БД:
Web of science: WOS:000329257000046
Scopus: 2-s2.0-84889094417
РИНЦ: 21464698
Chemical Abstracts: 2013:1271682
Chemical Abstracts (print): 160:101344
OpenAlex: W1973832952
Цитирование в БД:
БД Цитирований
Web of science 8
Scopus 7
РИНЦ 6
OpenAlex 6
Альметрики: