Sodium hexafluoroantimonate → Dibenzyl(phenyl)sulfanium hexafluoroantimonate(1-)

HRID 1886130Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1886130
F[B-](F)(F)F.[CH2:6]([SH+:13][CH2:14][C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1.[F:21][Sb-:22]([F:27])([F:26])([F:25])([F:24])[F:23].[Na+]>C(Cl)Cl>[F:21][Sb-:22]([F:27])([F:26])([F:25])([F:24])[F:23].[CH2:14]([S+:13]([CH2:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1)[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1)[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1

Komponenten

4

Edukt 2

HCID 16689647Sodium hexafluoroantimonateHCID 19877065HCID 19877065, Verbindung

Produkt 1

HCID 21263248Dibenzyl(phenyl)sulfanium hexafluoroantimonate(1-)Ausbeute 191,3 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel

Versuchsvorschrift

A mixture of 123.0 g (0.325 mol) of dibenzylsulfonium tetrafluoroborate in 400 ml of methylene chloride is dissolved in a 2 liter round-bottomed flask at RT under N2 to give a clear solution. 117.8 g of sodium hexafluoroantimonate are then added and the mixture is stirred at RT for 31/2 h. The suspension is now filtered over silica gel and the solvent is removed from the filtrate using a rotary evaporator. The slightly reddish viscous residue is dissolved again in 250 ml of methanol, and after addition of 250 ml of water the product is allowed to crystallize at RT for 1-2 h. The suspension is filtered and the residue is washed with water. The product is then dried under a high vacuum at RT overnight. 163.9 g (95% of theory) of dibenzylphenylsulfonium hexafluoroantimonate are obtained as white crystals of melting point 105°-109° C.

Aufarbeitung

  1. dissolutionis dissolved in a 2 liter round-bottomed flask at RT under N2
  2. customto give a clear solution
  3. filtrationThe suspension is now filtered over silica gel
  4. customthe solvent is removed from the filtrate
  5. customa rotary evaporator
  6. dissolutionThe slightly reddish viscous residue is dissolved again in 250 ml of methanol
  7. additionafter addition of 250 ml of water the product
  8. customto crystallize at RT for 1-2 h
  9. filtrationThe suspension is filtered
  10. washthe residue is washed with water
  11. customThe product is then dried under a high vacuum at RT overnight

Quellen und Nachweise

ORD-Eintrag
ord-758fbc23794545e98acc52c60347c6e6
Quelldatensatz
uspto-grants-1992_09
Patentnummer
US05149767

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