Reaktion #4048

ord-bced94d3b141486e89edeb33840b194b

Reaktionsgleichung

O=S(=O)(F)C(F)(F)C(F)(F)OC(F)(F)C(F)(F)F
perfluoro-3-oxapentanesulfonyl fluoride
C[Si](C)(C)[O-].[K+]
potassium trimethylsilanolate
C1CCOC1
tetrahydrofuran
O=S(=O)([O-])C(F)(F)C(F)(F)OC(F)(F)C(F)(F)F.[K+]
Potassium perfluoro-3-oxapentanesulfonate
Ausbeute 65.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturwhile heating
  2. 2
    Temperaturat reflux for 1.5 h
  3. 3
    EinengenPotassium perfluoro-3-oxapentanesulfonate (3.79 g initially and 1.74 g by concentrating the filtrate under vacuum
  4. 4
    Sonstigetotal 5.53 g, 65% yield) was isolated as a white solid

Vorschrift

The procedure of Example 1 was followed using perfluoro-3-oxapentanesulfonyl fluoride (7.95 g, 25 mmol), potassium trimethylsilanolate (3.2 g, 25 mmol) and dry tetrahydrofuran (100 mL) while heating at reflux for 1.5 h. Potassium perfluoro-3-oxapentanesulfonate (3.79 g initially and 1.74 g by concentrating the filtrate under vacuum; total 5.53 g, 65% yield) was isolated as a white solid: 19F NMR (fluorotrichloromethane) δ -79.4 (m, CF2, 2F), -83.2 (s, CF3, 3F), -84.9 (m, CF2, 2F), -115.0 ppm (m, CF2, 2F); Positive ion Fast Atom Bombardment MS (Glycerol matrix, Cs⊕ ion bombardment) m/e 393, 747, 1101, 1455, 1809 for M+K⊕ to M5 +K⊕.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04723016uspto-grants-1988_02