Sodium Carbonate → HCID 57264076, Verbindung

HRID 470725

Reaktionsgleichung

Reaktionsgleichung von HRID 470725
[CH3:1][O:2][C:3]1[C:8]([O:9][CH3:10])=[CH:7][CH:6]=[CH:5][C:4]=1B(O)O.[F:14][C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=1Br.C(=O)([O-])[O-].[Na+].[Na+]>COCCOC>[F:14][C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=1[C:4]1[CH:5]=[CH:6][CH:7]=[C:8]([O:9][CH3:10])[C:3]=1[O:2][CH3:1]

Komponenten

5

Edukt 3

HCID 10340Sodium CarbonateHCID 612591-Bromo-2-fluorobenzeneHCID 51564912,3-Dimethoxybenzeneboronic acid

Produkt 1

HCID 57264076HCID 57264076, VerbindungAusbeute 85 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 80711,2-DimethoxyethaneLösungsmittel

Versuchsvorschrift

In the atmosphere of argon, 18.2 g of 2,3-dimethoxyphenylboronic acid, 17.5 g of 2-fluorobromobenzene, 2.31 g of tetrakistriphenylphosphine palladium (0), 300 mL of 1,2-dimethoxyethane and 150 mL of an aqueous 2M sodium carbonate solution were placed in a flask. The resulting mixture was stirred with heating under reflux for 8 hours. After cooling to room temperature, an aqueous phase was removed, and an organic phase was washed with saturated saline. The organic phase was dried with magnesium sulfate and then concentrated. Residues were purified by silica gel column chromatography, whereby 19.7 g of (yield 85%) of 2′-fluoro-2,3-dimethoxybiphenyl was obtained.

Aufarbeitung

  1. temperaturewith heating
  2. temperatureunder reflux for 8 hours
  3. customan aqueous phase was removed
  4. washan organic phase was washed with saturated saline
  5. dry with materialThe organic phase was dried with magnesium sulfate
  6. concentrationconcentrated
  7. customResidues were purified by silica gel column chromatography

Quellen und Nachweise

ORD-Eintrag
ord-7945c7618e4a4cf3a4fa1638c02cf341
Quelldatensatz
uspto-grants-2014_01
Patentnummer
US08629430B2

Verknüpfte Notizen

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