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ChemicalBook--->CAS DataBase List--->1084334-86-0

1084334-86-0

1084334-86-0 Structure

1084334-86-0 Structure
IdentificationBack Directory
[Name]

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

1084334-86-0
[Synonyms]

BAPTPA
(4-([1,1'-biphenyl]-4-yl(phenyl)amino)phenyl)boronic acid
Boronic acid,B-[4-([1,1'-biphenyl]-4-ylphenylamino)phenyl]-
[Molecular Formula]

C24H20BNO2
[MDL Number]

MFCD28144504
[MOL File]

1084334-86-0.mol
[Molecular Weight]

365.232
Chemical PropertiesBack Directory
[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)
Hazard InformationBack Directory
[Synthesis]

N-(4-broMophenyl)-N-phenyl-[1,1'-Biphenyl]-4-aMine

503299-24-9

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

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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