Sodium Carbonate → 4-Fluoro-3'-methoxy-3-nitrobiphenyl
Reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5](B(O)O)[CH:6]=[CH:7][CH:8]=1.Br[C:13]1[CH:14]=[CH:15][C:16]([F:22])=[C:17]([N+:19]([O-:21])=[O:20])[CH:18]=1.C(=O)([O-])[O-].[Na+].[Na+]>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>[F:22][C:16]1[CH:15]=[CH:14][C:13]([C:5]2[CH:6]=[CH:7][CH:8]=[C:3]([O:2][CH3:1])[CH:4]=2)=[CH:18][C:17]=1[N+:19]([O-:21])=[O:20]Participants
7
Reactant 3
Product 1
Reagents, catalysts & solvents 3
Procedure
Tetrakis(triphenylphosphine)palladium (0.8 g) was added to a mixture of 5 g of 3-methoxyphenylboronic acid, 5 g of 5-bromo-2-fluoronitrobenzene and 11 mL of 2 M sodium carbonate solution in 100 mL of toluene. The mixture was heated to refulux for 2 hours, diluted with water and extracted with ethyl acetate. The ethyl acetate was washed with saturated sodium bicarbonate, brine, dried, and concentrated to give an oily solid. The solid was chromatographed on silica gel in ethyl acetate:hexane 1:6 to give 4.3 g (77% yield) of 4-fluoro-3′-methoxy-3-nitrobiphenyl.
Workup
- temperatureThe mixture was heated
- extractionextracted with ethyl acetate
- washThe ethyl acetate was washed with saturated sodium bicarbonate, brine
- customdried
- concentrationconcentrated
- customto give an oily solid
- customThe solid was chromatographed on silica gel in ethyl acetate:hexane 1:6
Sources & evidence
- ORD record
- ord-929df09169704fbea10ea535a35cd0b4
- Source dataset
- uspto-grants-2003_02
- Patent number
- US06514981B1
Reaction notes
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