Reaktion #3010

ord-36355329f50b4fba91d75f1d3bd8c47f

Reaktionsgleichung

[Cl-].c1ccc([S+](c2ccccc2)c2ccccc2)cc1
triphenylsulfonium chloride
ClCCl
dichloromethane
O=S(=O)(Cl)c1ccc(C(F)(F)F)cc1
4-trifluoromethylbenzenesulfonyl chloride
O=C([O-])[O-].[Na+].[Na+]
sodium carbonate
O=S(=O)([O-])c1ccc(C(F)(F)F)cc1.c1ccc([S+](c2ccccc2)c2ccccc2)cc1
triphenylsulfonium 4 -trifluoromethylbenzenesulfonate

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturwas heated
  2. 2
    Temperaturat reflux for 22 hours
  3. 3
    workup.STIRRINGthe mixture stirred at room temperature for 20 hours
  4. 4
    SonstigeThe layers were separated
  5. 5
    Waschenthe organic layer washed with water (7×150 ml) until the washings
  6. 6
    SonstigeAfter drying
  7. 7
    Sonstige(MgSO4 ), removal of the solvent in vacuo
  8. 8
    Sonstigegave a pale yellow foam which
  9. 9
    Sonstigewas further dried
  10. 10
    Temperaturby heating at 80°-100° C. for 108 hours under vacuum

Vorschrift

A suspension of 4-trifluoromethylbenzenesulfonyl chloride (20.53 g, 83.9 mmol) in water (150 ml) containing sodium carbonate (9.43 g, 88.10 mmol) was heated at reflux for 22 hours. After cooling to room temperature, triphenylsulfonium chloride (50% aqueous solution, 50.00 g) was added over 15 minutes. After stirring the biphasic mixture for 30 minutes, dichloromethane (300 ml) was added and the mixture stirred at room temperature for 20 hours. The layers were separated and the organic layer washed with water (7×150 ml) until the washings were neutral (pH 7 ). After drying (MgSO4 ), removal of the solvent in vacuo gave a pale yellow foam which was further dried by heating at 80°-100° C. for 108 hours under vacuum. In this way, triphenylsulfonium 4 -trifluoromethylbenzenesulfonate was isolated as a pale yellow glass (36.77 g).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05731364uspto-grants-1998_03