4-Fluorophenylboronic acid → Methyl 4-methoxy-2-(4-fluorophenyl)benzoate

HRID 1836423Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1836423
C(=O)([O-])O.[Na+].[CH3:6][O:7][C:8]1[CH:17]=[CH:16][C:11]([C:12]([O:14][CH3:15])=[O:13])=[C:10](S(C(F)(F)F)(=O)=O)[CH:9]=1.[F:25][C:26]1[CH:31]=[CH:30][C:29](B(O)O)=[CH:28][CH:27]=1>COCCOC.[Pd].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>[CH3:6][O:7][C:8]1[CH:17]=[CH:16][C:11]([C:12]([O:14][CH3:15])=[O:13])=[C:10]([C:29]2[CH:30]=[CH:31][C:26]([F:25])=[CH:27][CH:28]=2)[CH:9]=1

Komponenten

6

Versuchsvorschrift

Saturated aqueous sodium hydrogen carbonate solution (50 ml) was added to a solution of methyl 4-methoxy-2-trifluoromethanesulphonylbenzoate (6.3 g.) and 4-fluorobenzeneboronic acid (3.36 g.) in DME (150 ml) at ambient temperature under an argon atmosphere. Tetrakis(triphenylphosphine) palladium (928 mg.) was added and the reaction heated and stirred at reflux for 3.5 hours resulting in a homogeneous solution. After cooling to ambient temperature, the reaction was partitioned between ethyl acetate and water. The organic phase was washed with 2N hydrochloric acid, water and brine, filtered through 1PS filter paper and the solvent removed to give methyl 4-methoxy-2-(4-fluorophenyl)benzoate as a yellow-oily solid (7.2 g) which was used without further purification.

Aufarbeitung

  1. temperaturethe reaction heated
  2. temperatureat reflux for 3.5 hours
  3. customresulting in a homogeneous solution
  4. customthe reaction was partitioned between ethyl acetate and water
  5. washThe organic phase was washed with 2N hydrochloric acid, water and brine
  6. filtrationfiltered through 1PS filter paper
  7. customthe solvent removed

Quellen und Nachweise

ORD-Eintrag
ord-13bb38d1e4df4201a20264da3bfffdc2
Quelldatensatz
uspto-grants-2004_08
Patentnummer
US06777438B2

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