ChemicalBook--->CAS DataBase List--->35708-19-1

35708-19-1

35708-19-1 Structure

35708-19-1 Structure
IdentificationBack Directory
[Name]

2-Anilinobenzoic acid methyl ester
[CAS]

35708-19-1
[Synonyms]

METHYL 2-ANILINOBENZOATE
methyl 2-(phenylamino)benzoate
2-Anilinobenzoic acid methyl ester
2-(Phenylamino)benzoic acid methyl ester
Benzoic acid, 2-(phenylaMino)-, Methyl ester
[Molecular Formula]

C14H13NO2
[MDL Number]

MFCD01366532
[MOL File]

35708-19-1.mol
[Molecular Weight]

227.26
Chemical PropertiesBack Directory
[Melting point ]

58-59 °C
[Boiling point ]

140 °C(Press: 0.1 Torr)
[density ]

1.175±0.06 g/cm3(Predicted)
[storage temp. ]

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

-1.27±0.20(Predicted)
[Appearance]

Off-white to gray Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Spectrum DetailBack Directory
[Spectrum Detail]

2-Anilinobenzoic acid methyl ester(35708-19-1)1HNMR
Hazard InformationBack Directory
[Synthesis]

Bromobenzene

108-86-1

Methyl anthranilate

134-20-3

2-Anilinobenzoic acid methyl ester

35708-19-1

General procedure for the synthesis of methyl 2-aminobenzoate from bromobenzene and methyl o-aminobenzoate: 15 g of methyl o-aminobenzoate, 15.6 g of bromobenzene, 0.9 g of tris(dibenzylideneacetone)dipalladium (Pd2(dba)3), 0.4 g of tri-tert-butylphosphine (P(t-Bu)3), and 28.6 g of tertiary butylsodium alcohol (Na(t-BuO)) were added, under nitrogen protection, to a round bottom flask followed by addition of 100 mL of toluene as solvent. The mixture was stirred and heated to reflux. Upon completion of the reaction, the reaction mixture was cooled to room temperature and washed with dichloromethane and water. The organic layer was separated, dried over anhydrous magnesium sulfate (MgSO4), filtered and purified by column chromatography to give the final methyl 2-(phenylamino)benzoate in a yield of 21.0 g in 93%.

[References]

[1] Tetrahedron, 2006, vol. 62, # 48, p. 11100 - 11105
[2] Patent: TWI579270, 2017, B. Location in patent: Paragraph 0094; 0095
[3] Chemistry - A European Journal, 2006, vol. 12, # 13, p. 3636 - 3646
[4] Journal of Organic Chemistry, 2005, vol. 70, # 20, p. 8107 - 8109
[5] Patent: KR2016/102142, 2016, A. Location in patent: Paragraph 0215; 0218; 0219
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