Sodium Carbonate → 4-Fluoro-3'-methoxy-3-nitrobiphenyl

HRID 1860951Notes

Reaction equation

HRID 1860951 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

Procedure

Tetrakis(triphenylphosphine)palladium (0.7 g) was added to a mixture of 5 g of 3-methoxyphenylboronic acid, 3.8 g of 5-bromo-2-fluoronitrobenzene, and 11 mL of 2 M sodium carbonate solution in 100 mL of toluene. The mixture was refluxed for 2 hours, diluted with water and extracted with ethyl acetate. The ethyl acetate was washed with saturated sodium bicarbonate and brine, dried, and concentrated to give an oily solid. The solid was purified on a silica gel column using a 1:6 mixture of ethyl acetate:hexane as eluent, to give 4.3 g (77%) of 4-fluoro-3′-methoxy-3-nitrobiphenyl.

Workup

  1. temperatureThe mixture was refluxed for 2 hours
  2. extractionextracted with ethyl acetate
  3. washThe ethyl acetate was washed with saturated sodium bicarbonate and brine
  4. customdried
  5. concentrationconcentrated
  6. customto give an oily solid
  7. customThe solid was purified on a silica gel column
  8. additiona 1:6 mixture of ethyl acetate

Sources & evidence

ORD record
ord-dfa1127bb898453f84affc0b1d2c0f61
Source dataset
uspto-grants-2003_03
Patent number
US06531502B1

Reaction notes

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