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202831-65-0

202831-65-0 Structure

202831-65-0 Structure
IdentificationBack Directory
[Name]

4-BROMO-4'-(DIPHENYLAMINO)BIPHENYL
[CAS]

202831-65-0
[Synonyms]

K0063
4-BROMO-4'-(DIPHENYLAMINO)BIPHENYL
4-BROMO-4`-(DIPHENYLLAMINO)BIPHENYL
(4'-BROMOBIPHENYL-4-YL)DIPHENYLAMINE
4'-Bromo-N,N-diphenyl-4-biphenylamine
4'-broMo-N,N-diphenylbiphenyl-4-aMine
4-(4-bromophenyl)-N,N-diphenylaniline
4-Bromo-4'-(diphenylamino)biphenyl >
N,N-Diphenyl-4'-bromo-1,1'-biphenyl-4-amine
4-BROMO-4''-(DIPHENYLAMINO)BIPHENYL, 93%(GC)
4'-BroMo-N,N-diphenyl-[1,1'-biphenyl]-4-aMine
[1,1'-Biphenyl]-4-amine, 4'-bromo-N,N-diphenyl-
4'-BroMo-N,N-diphenyl-[1,1'-biphenyl]-4-aMine
[EINECS(EC#)]

1312995-182-4
[Molecular Formula]

C24H18BrN
[MDL Number]

MFCD09038499
[MOL File]

202831-65-0.mol
[Molecular Weight]

400.31
Chemical PropertiesBack Directory
[Melting point ]

127.0 to 131.0 °C
[Boiling point ]

518.2±33.0 °C(Predicted)
[density ]

1.325
[storage temp. ]

Keep in dark place,Sealed in dry,Room Temperature
[form ]

powder to crystal
[pka]

-3.34±0.60(Predicted)
[color ]

White to Orange to Green
Safety DataBack Directory
[HS Code ]

29214990
Hazard InformationBack Directory
[Synthesis]

1-Bromo-4-iodobenzene

589-87-7

4-(Diphenylamino)phenylboronic acid

201802-67-7

4-BROMO-4'-(DIPHENYLAMINO)BIPHENYL

202831-65-0

Example 1.13.1 Synthesis of 4'-bromo-N,N-diphenyl-[1,1'-biphenyl]-4-amine (35): (4-(diphenylamino)phenyl)boronic acid (1.5 g, 5.19 mmol), 4-iodo-1-bromobenzene (1.33 g, 4.71 mmol), Na2CO3 (1.78 g, 16.8 mmol) and Pd(PPh3 )4 (0.163 g, 0.141 mmol) were dissolved in THF/H2O (28 mL/17 mL) mixed solvent. The reaction mixture was degassed and heated to reflux under argon protection overnight. After completion of the reaction, it was cooled to room temperature and the mixture was poured into dichloromethane (150 mL) and washed sequentially with water (2 x 150 mL) and brine (100 mL). The organic phase was dried with Na2SO4, filtered and purified by fast column chromatography (silica gel, hexane/ethyl acetate 50:1), and finally recrystallized in a solvent mixture of dichloromethane/methanol to give a white solid product (compound 35) (1.64 g, 87% yield).

[References]

[1] Journal of Organic Chemistry, 2017, vol. 82, # 18, p. 9435 - 9451
[2] Patent: US2010/326526, 2010, A1
[3] Patent: WO2011/8560, 2011, A1. Location in patent: Page/Page column 47-48
[4] RSC Advances, 2015, vol. 5, # 41, p. 32298 - 32306
[5] Patent: US9172051, 2015, B2. Location in patent: Page/Page column 67; 68; 69; 70; 71; 72; 75; 76
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