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4445-43-6

4445-43-6 Structure

4445-43-6 Structure
IdentificationBack Directory
[Name]

3-AMINO-1,1'-BIPHENYL-4-CARBOXYLICACID
[CAS]

4445-43-6
[Synonyms]

2-Amino-4-phenylbenzoic acid
3-Amino-[1,1'-biphenyl]-4-carboxylic acid
[Molecular Formula]

C13H11NO2
[MDL Number]

MFCD00577380
[MOL File]

4445-43-6.mol
[Molecular Weight]

213.23
Chemical PropertiesBack Directory
[Melting point ]

202.6-203.8 °C(Solv: ethanol (64-17-5))
[Boiling point ]

427.0±45.0 °C(Predicted)
[density ]

1.257±0.06 g/cm3(Predicted)
[storage temp. ]

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

4.93±0.10(Predicted)
[Appearance]

Light brown to brown Solid
Spectrum DetailBack Directory
[Spectrum Detail]

3-AMINO-1,1'-BIPHENYL-4-CARBOXYLICACID(4445-43-6)1HNMR
Hazard InformationBack Directory
[Synthesis]

2-Amino-4-bromobenzoic acid

20776-50-5

Phenylboronic acid

98-80-6

3-AMINO-1,1'-BIPHENYL-4-CARBOXYLICACID

4445-43-6

Pd(PPh3)4 (0.052 g, 0.045 mmol) was added to degassed DMF (10 mL) and 1 M K2CO3 aqueous solution (7 mL) under nitrogen protection using 2-amino-4-bromobenzoic acid (0.992 g, 4.46 mmol) and phenylboronic acid (0.832 g, 6.69 mmol). The reaction mixture was stirred at 80 °C for 16 hours. Upon completion of the reaction, DMF was removed under reduced pressure.The residue was dissolved in 4 N NaOH aqueous solution (40 mL) and the aqueous phase was washed twice with ethyl acetate (2 x 50 mL). The pH of the aqueous phase was adjusted to 5 by the addition of 4 N HCl. Subsequently, the aqueous phase was extracted three times with ethyl acetate (3 x 50 mL) and once with DCM-MeOH (9:1, 50 mL). All organic phases were combined, dried with MgSO4, and the solvent was evaporated under reduced pressure to give a beige solid. The solid was ground in ether, filtered and dried to give 3-amino-[1,1'-biphenyl]-4-carboxylic acid as a beige solid (0.721 g, 76% yield). mS (ESI, m/z): 214.3 [M + H+] C13H11NO2; tR = 0.78 min.

[References]

[1] Patent: WO2015/173329, 2015, A1. Location in patent: Page/Page column 99
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