Reaction #2005
ord-eb2559d3fc404f17a5ecee988d37d685
Reaction equation
Reactants
Reagents
Solvents
Conditions
Workup
- 1TemperatureThe two-phase mixture was heated
- 2Temperatureat reflux for three hours
- 3OtherThe cooled reaction mixture
- 4Filtrationwas filtered through Celite
- 5Washthe filter cake washed with fresh benzene
- 6OtherThe organic layer was separated
- 7Washwashed with water (3×)
- 8Dryingdried over magnesium sulfate
- 9Filtrationfiltered
- 10OtherThe filtrate was evaporated under vacuum
- 11Otherthe residue (46.1 g) purified by preparative high pressure liquid chromatography on silica gel
- 12Washeluting with hexane/ethyl acetate (20:1)
Procedure
A vigorously stirred mixture of 34 g (0.25 mol) of 4-tolylboronic acid and 34 g (0.17 mol) of 2-bromo-1-nitrobenzene in a mixture of 170 mL of 5N sodium hydroxide, 57 mL of water, 215 mL of 2-propanol and 1080 mL of benzene was treated with 11.9 g of (tetrakis)triphenylphosphine palladium(0). The two-phase mixture was heated at reflux for three hours. The cooled reaction mixture was filtered through Celite and the filter cake washed with fresh benzene. The organic layer was separated and washed with water (3×), dried over magnesium sulfate and filtered. The filtrate was evaporated under vacuum and the residue (46.1 g) purified by preparative high pressure liquid chromatography on silica gel, eluting with hexane/ethyl acetate (20:1), to give 28.05 g of the product.