Реакция #216833

ord-6384164cd22146bd8e8ee6bce72735ff

Уравнение реакции

[Cl-].c1ccc([I+]c2ccccc2)cc1
diphenyliodonium chloride
Fc1c(F)c(F)c([B-](c2c(F)c(F)c(F)c(F)c2F)(c2c(F)c(F)c(F)c(F)c2F)c2c(F)c(F)c(F)c(F)c2F)c(F)c1F.[Li+]
lithium tetrakis(pentafluorophenyl)borate
Fc1c(F)c(F)c([B-](c2c(F)c(F)c(F)c(F)c2F)(c2c(F)c(F)c(F)c(F)c2F)c2c(F)c(F)c(F)c(F)c2F)c(F)c1F.c1ccc([I+]c2ccccc2)cc1
diphenyliodonium tetrakis(pentafluorophenyl)borate
Выход 75.0%

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ТемператураThe mixture was maintained
  2. 2
    Фильтрацияwas then filtered
  3. 3
    ДругоеThe filtrate was dried under reduced pressure (133 Pa) overnight with the exclusion of light
  4. 4
    Другое16.33 g (or a yield of 75%) of diphenyliodonium tetrakis(pentafluorophenyl)borate were thus recovered

Методика

7.17 g (or 22.6 mmol) of diphenyliodonium chloride were dissolved in 300 ml of water in a 1,000 ml Erlenmeyer flask. 15.52 g (or 22.6 mmol) of lithium tetrakis(pentafluorophenyl)borate in solution in 250 ml of water were added dropwise. The mixture was maintained under stirring for 30 minutes and was then filtered. The filtrate was dried under reduced pressure (133 Pa) overnight with the exclusion of light. 16.33 g (or a yield of 75%) of diphenyliodonium tetrakis(pentafluorophenyl)borate were thus recovered.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05468902uspto-grants-1995_11