Reaktion #1061897

ord-0017f2390d414d74bd6068e2c0f7ef96

Reaktionsgleichung

O=C(O)c1c(F)c(F)c(F)c(F)c1F
2,3,4,5,6-pentafluorobenzoic acid
OCC(F)(F)C(F)(F)C(F)(F)C(F)F
2,2,3,3,4,4,5,5-octafluoropentanol
O
water
[H-].[Na+]
sodium hydride
O=C(O)c1c(F)c(F)c(OCC(F)(F)C(F)(F)C(F)(F)C(F)F)c(F)c1F
4-(2,2,3,3,4,4,5,5-octafluoropentyloxy)-2,3,5,6-tetrafluorobenzoic acid
Ausbeute 46.2%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONwas added
  2. 2
    WaschenThe separated organic layer was washed with water and brine
  3. 3
    Trocknendried over magnesium sulfate
  4. 4
    Filtrationfiltered
  5. 5
    Sonstigeevaporated in vacuo
  6. 6
    SonstigeThe residue was purified by chromatography on silica gel

Vorschrift

To a mixture of 2,3,4,5,6-pentafluorobenzoic acid (1 g) and 2,2,3,3,4,4,5,5-octafluoropentanol (1.18 g) in N,N-dimethylformamide (5 ml) was added 62% sodium hydride (0.39 g) at room temperature. The mixture was stirred at the same temperature for 1 hour, and thereto was added a mixture of water and ethyl acetate. The separated organic layer was washed with water and brine, dried over magnesium sulfate, filtered, and evaporated in vacuo. The residue was purified by chromatography on silica gel to give 4-(2,2,3,3,4,4,5,5-octafluoropentyloxy)-2,3,5,6-tetrafluorobenzoic acid (923.0 mg).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: USH0001638uspto-grants-1997_03