Sodium Carbonate → 2-Bromo-4'-chloro-1,1'-biphenyl

HRID 1771164Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1771164
C(=O)([O-])[O-].[Na+].[Na+].Br[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=1[Br:14].[Cl:15][C:16]1[CH:21]=[CH:20][C:19](B(O)O)=[CH:18][CH:17]=1>C1(C)C=CC=CC=1.O.C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>[Br:14][C:9]1[CH:10]=[CH:11][CH:12]=[CH:13][C:8]=1[C:19]1[CH:20]=[CH:21][C:16]([Cl:15])=[CH:17][CH:18]=1

Komponenten

7

Versuchsvorschrift

Sodium carbonate (19.8 g, 186.81 mmol) and tetrakis(triphenylphosphine)palladium(0) (1.05 g, 0.90 mmol) were added to a solution of 1,2-dibromobenzene (12.8 ml, 105.98 mmol) and 4-chlorophenylboronic acid (14.1 g, 90.08 mmol) in toluene (170 ml) and water (80 ml). The mixture was purged with nitrogen and heated at reflux overnight. The reaction mixture was allowed to cool to room temperature, and partitioned between saturated aq. NH4Cl and ethyl acetate (500 ml). The organic layer was dried over MgSO4, filtered and the volatiles were evaporated under reduced pressure to give a residue. The residue was purified by column chromatography (ISCO, 330 g silica gel column, eluting with 100% hexanes) to give the title product (17.0 g, yield: 71%).

Aufarbeitung

  1. customThe mixture was purged with nitrogen
  2. temperatureheated
  3. temperatureat reflux overnight
  4. custompartitioned between saturated aq. NH4Cl and ethyl acetate (500 ml)
  5. dry with materialThe organic layer was dried over MgSO4
  6. filtrationfiltered
  7. customthe volatiles were evaporated under reduced pressure
  8. customto give a residue
  9. customThe residue was purified by column chromatography (ISCO, 330 g silica gel column, eluting with 100% hexanes)

Quellen und Nachweise

ORD-Eintrag
ord-01b486c1d603417ba4a6110b0daa5754
Quelldatensatz
uspto-grants-2016_02
Patentnummer
US09248140B2

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