Solvent-Free Fluorination of Electron-Rich Aromatic Compounds with F-TEDA-BF4: Toward "Dry" Processes Научная публикация
Журнал |
European Journal of Organic Chemistry
ISSN: 1434-193X , E-ISSN: 1099-0690 |
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Вых. Данные | Год: 2017, Том: 2017, Номер: 17, Страницы: 2469-2474 Страниц : 6 DOI: 10.1002/ejoc.201700179 | ||||||
Ключевые слова | Aromatic substitution; Electrophilic substitution; Fluorine; Solid-state reactions; Sustainable chemistry | ||||||
Авторы |
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Организации |
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Реферат:
An effective protocol for the solvent-free fluorination of electron-rich aromatic compounds with 1-chloromethyl-4-fluoro-1,4-diazoniabicyclo[2.2.2]octane bis(tetrafluoroborate) (F-TEDA-BF4) is described. The protocol allows the easy and efficient isolation of fluorinated products in high yields and purities with low E factors (kg(waste)kg(product)(-1)) by vacuum-sublimation without the use of any solvent. The solid-state fluorination of naphthalen-2-ol was studied by differential thermal analysis, and scanning electron microscopy was used to obtain evidence for the solid-state process. The crucial influence of alkali-metal carbonates on the rate of the solvent-free fluorination of hydroxynaphthalenes and estrone was demonstrated.
Библиографическая ссылка:
Zaikin P.A.
, Dyan O.T.
, Evtushok D.V.
, Usoltsev A.N.
, Borodkin G.I.
, Karpova E.V.
, Shubin V.G.
Solvent-Free Fluorination of Electron-Rich Aromatic Compounds with F-TEDA-BF4: Toward "Dry" Processes
European Journal of Organic Chemistry. 2017. V.2017. N17. P.2469-2474. DOI: 10.1002/ejoc.201700179 WOS Scopus РИНЦ
Solvent-Free Fluorination of Electron-Rich Aromatic Compounds with F-TEDA-BF4: Toward "Dry" Processes
European Journal of Organic Chemistry. 2017. V.2017. N17. P.2469-2474. DOI: 10.1002/ejoc.201700179 WOS Scopus РИНЦ
Даты:
Опубликована в печати: | 3 мая 2017 г. |
Опубликована online: | 3 мая 2017 г. |
Идентификаторы:
Web of science | WOS:000400993800010 |
Scopus | 2-s2.0-85019018583 |
РИНЦ | 31038665 |
OpenAlex | W2593233388 |