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1,4-Dibromobenzene → 4'-Bromo[1,1'-biphenyl]-3-amine

HRID 253013
Notes
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Reaction equation

HRID 253013 reaction equation
Br[C:2]1[CH:7]=[CH:6][C:5]([Br:8])=[CH:4][CH:3]=1.[NH2:9][C:10]1[CH:11]=[C:12](B(O)O)[CH:13]=[CH:14][CH:15]=1.C(=O)([O-])[O-].[Na+].[Na+].C(OCC)(=O)C>CN(C)C=O.O>[Br:8][C:5]1[CH:6]=[CH:7][C:2]([C:14]2[CH:13]=[CH:12][CH:11]=[C:10]([NH2:9])[CH:15]=2)=[CH:3][CH:4]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

7

Reactant 4

HCID 78041,4-DibromobenzeneHCID 8857Ethyl AcetateHCID 10340Sodium CarbonateHCID 922693-Aminophenylboronic acid

Product 1

HCID 289112884'-Bromo[1,1'-biphenyl]-3-amineYield 57%

Reagents, catalysts & solvents 2

HCID 962
Water
Solvent
2×
HCID 6228DimethylformamideSolvent

Conditions

Temperature
80 °C

Procedure

1,4-Dibromobenzene (311 mg, 1.3 mmol) and 201 mg (1.3 mmol) of 3-aminophenylboronic acid were dissolved in 17 ml of N,N-dimethylformamide and 4.2 ml of water. Tetrakistriphenylphosphine palladium (154 mg, 0.13 mmol) and 211 mg (2.0 mmol) of sodium carbonate were added to the solution, and the mixture was stirred at 80° C. for 3 hr. Ethyl acetate (60 ml) and 8.5 ml of water were added to the reaction solution, and the mixture was filtered through Celite. The organic layer as the filtrate was washed five times with 30 ml of water. The organic layer was dried over anhydrous sodium sulfate and was filtered. The solvent was then removed by distillation. The residue was purified by column chromatography on silica gel (n-hexane:ethyl acetate=5:1) to give 182 mg (yield 57%) of the title compound.

Workup

  1. filtrationthe mixture was filtered through Celite
  2. washThe organic layer as the filtrate was washed five times with 30 ml of water
  3. dry with materialThe organic layer was dried over anhydrous sodium sulfate
  4. filtrationwas filtered
  5. customThe solvent was then removed by distillation
  6. customThe residue was purified by column chromatography on silica gel (n-hexane:ethyl acetate=5:1)

Sources & evidence

ORD record
ord-6edd673a2769430eb84b816708ba0fdf
Source dataset
uspto-grants-2011_01
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07871982B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes