ChemicalBook--->CAS DataBase List--->5129-23-7

5129-23-7

5129-23-7 Structure

5129-23-7 Structure
IdentificationBack Directory
[Name]

3-AMINO-4-ETHYLBENZOIC ACID
[CAS]

5129-23-7
[Synonyms]

BUTTPARK 121\11-46
3-AMINO-4-ETHYLBENZOIC ACID
Benzoic acid, 3-amino-4-ethyl-
3-AMINO-4-ETHYLBENZOIC ACID, 98+%
[Molecular Formula]

C9H11NO2
[MDL Number]

MFCD07774227
[MOL File]

5129-23-7.mol
[Molecular Weight]

165.19
Chemical PropertiesBack Directory
[Melting point ]

149.4-149.7 °C(Solv: water (7732-18-5))
[Boiling point ]

349.0±35.0 °C(Predicted)
[density ]

1.205±0.06 g/cm3(Predicted)
[storage temp. ]

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

4.52±0.10(Predicted)
[Appearance]

Light yellow to brown Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H335-H319
[Precautionary statements ]

P264-P280-P305+P351+P338-P337+P313P-P264-P280-P302+P352-P321-P332+P313-P362
Spectrum DetailBack Directory
[Spectrum Detail]

3-AMINO-4-ETHYLBENZOIC ACID(5129-23-7)1HNMR
Hazard InformationBack Directory
[Synthesis]

4-ETHYL-3-NITROBENZOIC ACID

103440-95-5

3-AMINO-4-ETHYLBENZOIC ACID

5129-23-7

General procedure for the preparation of Example 39-2 3-amino-4-ethylbenzoic acid: 4-ethyl-3-nitrobenzoic acid (5.0 g, 27.4 mmol) was dissolved in methanol (50 ml) and 5% Pd-C catalyst (250 mg) was added. The reaction mixture was gradually warmed from 0 °C to room temperature and stirred for 1 h under hydrogen atmosphere. After completion of the reaction, the catalyst was removed by filtration and the filtrate was concentrated under reduced pressure. The resulting crystals were washed with mixed methyl tert-butyl ether/hexane solvent and dried to give 3-ethyl-4-aminobenzoic acid (3.2 g, 70.6% yield). The product was characterized by 1H-NMR (DMSO-d6, δ ppm): 12.40 (1H, brs), 7.21 (1H, d, J = 1.6Hz), 7.07 (1H, dd, J = 1.6 and 7.6Hz), 6.99 (1H, d, J = 7.7Hz), 5.06 (2H, brs), 2.45 (2H, quartet peak, J = 7.4 Hz), 1.11 (3H, t, J = 7.4 Hz).

[References]

[1] Patent: US6348474, 2002, B1. Location in patent: Page column 80
[2] Journal of the American Chemical Society, 1950, vol. 72, p. 2807
[3] Chemische Berichte, 1971, vol. 104, # 9, p. 2751 - 2771
[4] Patent: WO2015/84606, 2015, A1. Location in patent: Page/Page column 129
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