ChemicalBook--->CAS DataBase List--->167218-30-6

167218-30-6

167218-30-6 Structure

167218-30-6 Structure
IdentificationBack Directory
[Name]

N,N,N'-Triphenyl-4,4'-bianiline
[CAS]

167218-30-6
[Synonyms]

N,N,N'-Triphenylbenz
N,N,N'-Triphenylbenzidine
N,N,N'-Triphenyl-4,4'-bianiline
4-Diphenylamino-4'-phenylaminobiphenyl
N4,N4,N4'-TRIPHENYL-BIPHENYL-4,4'-DIAMINE
N,N,N'-Triphenyl-[1,1'-biphenyl]-4,4'-diamine
N-phenyl-4-[4-(N-phenylanilino)phenyl]aniline
N,N,N'-Triphenylbenzidine
[1,1'-Biphenyl]-4,4'-diaMine, N,N,N'-triphenyl-
N4,N4,N4'-Triphenyl-[1,1'-biphenyl]-4,4'-diaMine
[1,1'-Biphenyl]-4,4'-diamine, N4,N4,N4'-triphenyl-
N-[4-(Diphenylamino)-1,1'-biphenyl-4'-yl]phenylamine
[Molecular Formula]

C30H24N2
[MDL Number]

MFCD17926476
[MOL File]

167218-30-6.mol
[Molecular Weight]

412.525
Chemical PropertiesBack Directory
[Melting point ]

168-169℃
[Boiling point ]

593.9±43.0 °C(Predicted)
[density ]

1.172
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
[form ]

powder to crystal
[pka]

0.90±0.40(Predicted)
[color ]

Light orange to Yellow to Green
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319
[Precautionary statements ]

P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313
[HS Code ]

2921.59.8090
Spectrum DetailBack Directory
[Spectrum Detail]

N,N,N'-Triphenyl-4,4'-bianiline(167218-30-6)1HNMR
Hazard InformationBack Directory
[Synthesis]

4-chloro-4'-(diphenylaMino)biphenyl

880800-25-9

Aniline

62-53-3

N,N,N'-Triphenyl-4,4'-bianiline

167218-30-6

To 4'-chloro-N,N-diphenyl-[1,1'-biphenyl]-4-amine (17.7 g, 50 mmol) and aniline (7 g, 75 mmol) was added dry toluene (150 ml) in a 250 ml two-neck flask. Palladium acetate (0.56 g, 2.5 mmol), t-Bu3P (0.225 g, 2.5 mmol) and sodium tert-butoxide (9.8 g, 100 mmol) were then added and the reaction was carried out at 125 °C for 10 hours. Upon completion of the reaction, 50 mL of water was added to quench the reaction and then extracted with ethyl acetate (150 mL). The organic phase was dried over anhydrous sodium sulfate, filtered and concentrated. Purification by column chromatography (petroleum ether: dichloromethane = 1:2) afforded the yellow solid product N,N,N'-triphenylbenzidine (17.9 g, 43.4 mmol, 86.9% yield).

[References]

[1] Patent: CN108570050, 2018, A. Location in patent: Paragraph 0071; 0073-0075
[2] Patent: WO2008/66358, 2008, A1. Location in patent: Page/Page column 54
[3] Patent: WO2008/133459, 2008, A1. Location in patent: Page/Page column 56
[4] Patent: US2010/65828, 2010, A1. Location in patent: Page/Page column 121
[5] Patent: US2010/65827, 2010, A1. Location in patent: Page/Page column 116
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