Sodium Carbonate → 3'-Methyl-biphenyl-4-carboxylic acid ethyl ester

HRID 1070417

Reaktionsgleichung

Reaktionsgleichung von HRID 1070417
[CH2:1]([O:3][C:4](=[O:12])[C:5]1[CH:10]=[CH:9][C:8](Br)=[CH:7][CH:6]=1)[CH3:2].[CH3:13][C:14]1[CH:15]=[C:16](B(O)O)[CH:17]=[CH:18][CH:19]=1.C(=O)([O-])[O-].[Na+].[Na+]>C1(C)C=CC=CC=1.[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>[CH2:1]([O:3][C:4]([C:5]1[CH:10]=[CH:9][C:8]([C:18]2[CH:17]=[CH:16][CH:15]=[C:14]([CH3:13])[CH:19]=2)=[CH:7][CH:6]=1)=[O:12])[CH3:2]

Komponenten

6

Edukt 3

HCID 10340Sodium CarbonateHCID 22043Ethyl 4-bromobenzoateHCID 27339503-Tolylboronic acid

Produkt 1

HCID 208200733'-Methyl-biphenyl-4-carboxylic acid ethyl esterAusbeute 87,3 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 11979704Tetrakis(triphenylphosphine)palladiumKatalysatorHCID 1140TolueneLösungsmittel

Reaktionsbedingungen

Temperatur
100 °C

Versuchsvorschrift

A mixture of 4-bromo benzoic acid ethyl ester (2.7 mL, 16.5 mmol), 3-methyl phenylboronic acid (2.2 g, 16.2 mmol) and sodium carbonate (7.5 g, 70.8 mmol) in toluene:ethanol:water (75 mL:37 mL:37 mL), was flushed with nitrogen for 1 hour. After addition of the tetrakis(triphenylphosphine) palladium(0) catalyst (0.94 g, 0.81 mmol), the reaction was heated at 100° C. overnight. After cooling, the mixture was filtered through Celite which was then washed with ethyl acetate. The organic layer was washed with water, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo to give a brown oil. Purification of the residue by flash chromatography with a solvent gradient from 25% to 50% of dichloromethane in hexane provided the title compound (3.4 g, 87.3%) as a colorless oil.

Aufarbeitung

  1. customethanol:water (75 mL:37 mL:37 mL), was flushed with nitrogen for 1 hour
  2. temperatureAfter cooling
  3. filtrationthe mixture was filtered through Celite which
  4. washwas then washed with ethyl acetate
  5. washThe organic layer was washed with water
  6. dry with materialdried over anhydrous sodium sulfate
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo
  9. customto give a brown oil
  10. customPurification of the residue by flash chromatography with a solvent gradient from 25% to 50% of dichloromethane in hexane

Quellen und Nachweise

ORD-Eintrag
ord-83c9807c4a224ca1b7368b37d9cb11f8
Quelldatensatz
uspto-grants-2005_06
Patentnummer
US06903091B2

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