Basic information Safety Supplier Related

B-[4-([1,1'-Biphenyl]-4-ylphenylaMino)phenyl]boronic acid

Basic information Safety Supplier Related

B-[4-([1,1'-Biphenyl]-4-ylphenylaMino)phenyl]boronic acid Basic information

Product Name:
B-[4-([1,1'-Biphenyl]-4-ylphenylaMino)phenyl]boronic acid
Synonyms:
  • (4-([1,1'-biphenyl]-4-yl(phenyl)amino)phenyl)boronic acid
  • Boronic acid,B-[4-([1,1'-biphenyl]-4-ylphenylamino)phenyl]-
  • BAPTPA
  • B-[4-([1,1'-Biphenyl]-4-ylphenylaMino)phenyl]boronic acid BAPTPA
  • B-[4-([1,1’-biphenyl]-4-ylphenylamino)phenyl]-Boronic acid
CAS:
1084334-86-0
MF:
C24H20BNO2
MW:
365.2321
Mol File:
1084334-86-0.mol
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B-[4-([1,1'-Biphenyl]-4-ylphenylaMino)phenyl]boronic acid Chemical Properties

Boiling point:
587.9±60.0 °C(Predicted)
Density 
1.25±0.1 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
8.61±0.16(Predicted)
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B-[4-([1,1'-Biphenyl]-4-ylphenylaMino)phenyl]boronic acid Usage And Synthesis

Synthesis

503299-24-9

1084334-86-0

2-2. Preparation of Compound 10: N-(4-bromophenyl)-N-phenyl-[1,1'-biphenyl]-4-amine (15.0 g, 37.5 mmol) was dissolved in tetrahydrofuran (190.0 mL) and n-butyllithium (2.5 M hexane solution, 22.0 mL) was slowly added to the solution at -78°C. After the reaction mixture was stirred at -78 °C for 1 h, trimethoxyborane (6.3 mL, 56.21 mmol) was added. Subsequently, the reaction mixture was warmed to room temperature and stirring was continued for 4 hours. Upon completion of the reaction, the mixture was extracted with ethyl acetate (200.0 mL) and the organic layer was washed with distilled water (100.0 mL). The organic solvent was removed by concentration under reduced pressure and the solid obtained was washed with hexane, filtered and dried to give 4-[N-(biphenyl-4-yl)-N-phenylamino]phenylboronic acid (10.0 g, 73% yield).

References

[1] Patent: WO2014/104704, 2014, A1. Location in patent: Paragraph 172-173
[2] Patent: US2013/76237, 2013, A1. Location in patent: Paragraph 0200; 0201

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