Potassium Carbonate → Methyl 4'-fluoro-1,1'-biphenyl-4-carboxylate

HRID 1741721Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1741721
I[C:2]1[CH:11]=[CH:10][C:5]([C:6]([O:8][CH3:9])=[O:7])=[CH:4][CH:3]=1.[F:12][C:13]1[CH:18]=[CH:17][C:16](B(O)O)=[CH:15][CH:14]=1.C([O-])([O-])=O.[K+].[K+]>CN(C=O)C.C([O-])(=O)C.[Pd+2].C([O-])(=O)C>[F:12][C:13]1[CH:18]=[CH:17][C:16]([C:2]2[CH:11]=[CH:10][C:5]([C:6]([O:8][CH3:9])=[O:7])=[CH:4][CH:3]=2)=[CH:15][CH:14]=1

Komponenten

6

Versuchsvorschrift

A solution of 1,1 '-bis(diphenylphosphine)-ferrocene (1.69 g, 3.05 mmol) and palladium acetate (515 mg, 2.29 mmol) in DMF (250 ml), is heated at 50° for 10 minutes. After the solution has cooled to room temperature methyl p-iodobenzoate (20 g, 76 mmol), 4-fluorobenzenboronic acid (20 g, 143 mmol) and K2CO3 (15.8 g, 114 mmol) are added. The resulting mixture is then heated to 90° for 24 hours. After once again cooling to room temperature the reaction mixture is filtered through Celite and the flitrate washed with EtOAc (3×100 ml). The combined organic portions are then washed with 2N HCl (100 ml), saturated NaCl solution (100 ml), 1N NaOH (100 ml), dried over MgSO4, and concentrated in vacuo. The resulting brown solid is chromatographed (silica gel; hexanes, 1% EtOAc/hexanes) to afford methyl 4'-fluoro-4-biphenylyl-carboxylate as a white solid.

Aufarbeitung

  1. additionare added
  2. temperatureThe resulting mixture is then heated to 90° for 24 hours
  3. filtrationis filtered through Celite
  4. washthe flitrate washed with EtOAc (3×100 ml)
  5. washThe combined organic portions are then washed with 2N HCl (100 ml), saturated NaCl solution (100 ml), 1N NaOH (100 ml)
  6. dry with materialdried over MgSO4
  7. concentrationconcentrated in vacuo
  8. customThe resulting brown solid is chromatographed (silica gel; hexanes, 1% EtOAc/hexanes)

Quellen und Nachweise

ORD-Eintrag
ord-b43a6d4efc014664b18a2425cad9eb16
Quelldatensatz
uspto-grants-1994_08
Patentnummer
US05334600

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