Английская Википедия:Cyanuric fluoride

Материал из Онлайн справочника
Версия от 10:39, 23 февраля 2024; EducationBot (обсуждение | вклад) (Новая страница: «{{Английская Википедия/Панель перехода}} {{chembox | Watchedfields = changed | verifiedrevid = 421445376 | ImageFileL1 = Cyanuric fluoride.svg | ImageSizeL1 = 120 | ImageAltL1 = Skeletal formula of cyanuric fluoride | ImageFileR1 = Cyanuric-fluoride-3D-spacefill.png | ImageSizeR1 = 130 | ImageAltR1 = Space-filling model of the cyanuric fluoride molecule | IUPACName = 2,4,6-trifluoro-1,3,5-triazine | OtherNames = trifluorotria...»)
(разн.) ← Предыдущая версия | Текущая версия (разн.) | Следующая версия → (разн.)
Перейти к навигацииПерейти к поиску

Шаблон:Chembox Cyanuric fluoride or 2,4,6-trifluoro-1,3,5-triazine is a chemical compound with the formula (CNF)3. It is a colourless, pungent liquid. It has been used as a precursor for fibre-reactive dyes, as a specific reagent for tyrosine residues in enzymes, and as a fluorinating agent.[1]

It is classified as an extremely hazardous substance in the United States as defined in Section 302 of the U.S. Emergency Planning and Community Right-to-Know Act (42 U.S.C. 11002), and is subject to strict reporting requirements by facilities which produce, store, or use it in significant quantities.[2]

Preparation and reactions

Cyanuric fluoride is prepared by fluorinating cyanuric chloride. The fluorinating agent may be SbF3Cl2,[3] KSO2F,[4] or NaF.[5][6]

Cyanuric fluoride is used for the mild and direct conversion of carboxylic acids to acyl fluorides:[7]

Файл:Fluorination with cyanuric fluoride.svg

Other fluorinating methods are less direct and may be incompatible with some functional groups.[8]

Cyanuric fluoride hydrolyses easily to cyanuric acid and it reacts more readily with nucleophiles than cyanuric chloride.[4] Pyrolysis of cyanuric fluoride at 1300 °C is a way to prepare cyanogen fluoride:[9]

(CNF)3 → 3 CNF.

References