Reaction #586153

ord-86dcc9b859f34b799c80b133dbbf25f6

Reaction equation

OB(O)c1ccc(Cl)cc1Cl
2,4-dichlorophenylboronic acid
N#Cc1ccc(Br)cc1F
4-bromo-2-fluorobenzonitrile
O=C([O-])[O-].[Na+].[Na+]
sodium carbonate
Cc1ccccc1
toluene
N#Cc1ccc(-c2ccc(Cl)cc2Cl)cc1F
2-fluoro-4-(2,4-dichlorophenyl)benzonitrile
Yield 94.0%

Solvents

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    Temperatureunder reflux
  2. 2
    Temperaturewith heating for 2 hours
  3. 3
    workup.ADDITIONThe reaction mixture was poured into ice-cold water
  4. 4
    Extractionextracted with toluene
  5. 5
    WashThe toluene layer was washed with water twice
  6. 6
    Dryingdried over anhydrous magnesium sulfate
  7. 7
    workup.DISTILLATIONThe solvent was distilled off under reduced pressure

Procedure

1.0 g (5.2 mmol) of 2,4-dichlorophenylboronic acid, 1.1 g (5.5 mmol) of 4-bromo-2-fluorobenzonitrile, 1.6 g (15.0 mmol) of sodium carbonate and 0.8 g (0.7 mmol) of tetrakis(triphenylphosphine) palladium were added to a solvent mixture of 50 ml of toluene, 25 ml of ethanol and 25 ml of water, and the reaction was carried out under reflux with heating for 2 hours. The reaction mixture was poured into ice-cold water and extracted with toluene. The toluene layer was washed with water twice and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure to obtain 1.3 g of 2-fluoro-4-(2,4-dichlorophenyl)benzonitrile (yield 93.0%), which was used in Example 8 (1) as the starting material.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07767626B2uspto-grants-2010_08