Tetrafluoroboric acid → Diphenyliodonium Tetrafluoroborate

HRID 377381Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 377381
[F:1][B-:2]([F:5])([F:4])[F:3].[H+].P(O)(O)O.[Cl-].[C:12]1([I+:18][C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1>O.F[B-](F)(F)F.[Ag+]>[F:1][B-:2]([F:5])([F:4])[F:3].[C:19]1([I+:18][C:12]2[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=2)[CH:20]=[CH:21][CH:22]=[CH:23][CH:24]=1

Komponenten

6

Edukt 3

HCID 28118Tetrafluoroboric acidHCID 73870Diphenyliodonium chlorideHCID 107909Phosphorous acid

Produkt 1

HCID 11122160Diphenyliodonium Tetrafluoroborate

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 159722Silver tetrafluoroborateKatalysatorHCID 962WaterLösungsmittel

Versuchsvorschrift

The aromatic iodonium complex salts may be prepared by metathesis of corresponding aromatic iodonium simple salts (such as, for example, diphenyliodonium bisulfate) in accordance with the teachings of Beringer et al., J. Am. Chem. Soc. 81,342 (1959). Thus, for example, the complex salt diphenyliodonium tetrafluoroborate is prepared by the addition at 60° C. of an aqueous solution containing 29.2 g silver fluoroborate, 2 g fluoroboric acid, and 0.5 g phosphorous acid in about 30 ml of water to a solution of 44 g (139 millimoles) of diphenyliodonium chloride. The silver halide that precipitates is filtered off and the filtrate concentrated to yield diphenyliodonium fluoroborate which may be purified by recrystallization.

Aufarbeitung

  1. customis prepared by the addition at 60° C. of an aqueous solution
  2. customThe silver halide that precipitates
  3. filtrationis filtered off
  4. concentrationthe filtrate concentrated

Quellen und Nachweise

ORD-Eintrag
ord-7b4fbea1ae234166b84ecd963572eec5
Quelldatensatz
uspto-grants-2000_02
Patentnummer
US06025406

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