ChemicalBook--->CAS DataBase List--->2479-47-2

2479-47-2

2479-47-2 Structure

2479-47-2 Structure
IdentificationBack Directory
[Name]

2,2-Bis(4-aminophenyl)propane
[CAS]

2479-47-2
[Synonyms]

4,4'-(Propane-2,2-diyl)
4,4'-isopropylidenedianiline
4,4'-Isopropylidenebisaniline
2,2-Bis(4-aminophenyl)propane
2,2-Bis(p-aminophenyl)propane
4,4'-Dimethylmethylenebisaniline
4,4'-(Propane-2,2-diyl)dianiline
4,4'-(1-Methylethylidene)dianiline
3-(4-aminophenyl)-4-propan-2-ylaniline
4-[2-(4-aminophenyl)propan-2-yl]aniline
4-[2-(4-azanylphenyl)propan-2-yl]aniline
Benzenamine, 4,4'-(1-methylethylidene)bis-
4-[1-(4-Aminophenyl)-1-methylethyl]aniline
4-(2-(4-aminophenyl)propan-2-yl)benzenamine
[4-[1-(4-aminophenyl)-1-methyl-ethyl]phenyl]amine
2,2-Bis(4-aminophenyl)propane, 4,4'-Isopropylidenedianiline
[EINECS(EC#)]

219-612-6
[Molecular Formula]

C15H18N2
[MDL Number]

MFCD00438683
[MOL File]

2479-47-2.mol
[Molecular Weight]

226.32
Chemical PropertiesBack Directory
[Melting point ]

128.2-129.6 °C(Solv: benzene (71-43-2))
[Boiling point ]

200-231 °C(Press: 5.5 Torr)
[density ]

1.091±0.06 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2–8 °C
[pka]

5.51±0.25(Predicted)
[Appearance]

Light brown to gray Solid
[EPA Substance Registry System]

Benzenamine, 4,4'-(1-methylethylidene)bis- (2479-47-2)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302
[Precautionary statements ]

P280-P305+P351+P338
[HS Code ]

2921599090
Spectrum DetailBack Directory
[Spectrum Detail]

2,2-Bis(4-aminophenyl)propane(2479-47-2)1HNMR
Hazard InformationBack Directory
[Synthesis]

Aniline hydrochloride

142-04-1

Acetone

67-64-1

2,2-Bis(4-aminophenyl)propane

2479-47-2

In a 1 L autoclave, 500 g of aniline hydrochloride, 199 g of water and 80 g of acetone were added sequentially. The reaction mixture was heated to 160 °C and maintained under continuous stirring conditions for 18 hours. Upon completion of the reaction, the reaction system was cooled and the reaction solution was transferred to a 3L dispensing funnel and diluted with 1600 g of ethyl acetate and 200 g of water. Subsequently, 356 g of 48 wt% aqueous sodium hydroxide solution was added to the partition funnel for alkaline treatment. After separating the organic layer, the organic layer was washed with 745 g of water. The organic layer was quantitatively analyzed by gas chromatography with hexadecane as the internal standard. Ultimately, 249 g of 2,2-bis(4-aminophenyl)propane was prepared in 80% yield based on the molar feed of acetone.

[References]

[1] Patent: JP5707935, 2015, B2. Location in patent: Paragraph 0025
[2] Fortschr. Teerfarbenfabr. Verw. Industriezweige, vol. 14, p. 721
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