ChemicalBook--->CAS DataBase List--->2475-80-1

2475-80-1

2475-80-1 Structure

2475-80-1 Structure
IdentificationBack Directory
[Name]

METHYL 2-AMINO-5-METHOXYBENZOATE
[CAS]

2475-80-1
[Synonyms]

Methyl 6-amino-m-anisate
Methyl 5-methoxyanthranilate
Methyl2-amino-5-methoxybenzoate,96%
2-Amino-5-methoxybenzoic acid methyl ester
Benzoic acid, 2-aMino-5-Methoxy-, Methyl ester
[Molecular Formula]

C9H11NO3
[MDL Number]

MFCD09038482
[MOL File]

2475-80-1.mol
[Molecular Weight]

181.19
Chemical PropertiesBack Directory
[Melting point ]

37-38℃
[Boiling point ]

298.8±20.0 °C(Predicted)
[density ]

1.179±0.06 g/cm3(Predicted)
[storage temp. ]

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

2.70±0.10(Predicted)
[Appearance]

Light brown to brown Solid
[Water Solubility ]

Slightly Soluble (1.1 g/L) (25°C) in water.
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P280a-P304+P340-P305+P351+P338-P405-P501a
[HS Code ]

2922500090
Hazard InformationBack Directory
[Uses]

It is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuffs.
[Synthesis]

Methyl 5-methoxy-2-nitrobenzoate

2327-45-9

METHYL 2-AMINO-5-METHOXYBENZOATE

2475-80-1

The general procedure for the synthesis of methyl 2-amino-5-methoxybenzoate from methyl 5-methoxy-2-nitrobenzoate was as follows: methyl 5-methoxy-2-nitrobenzoate (1.60 g, 7.58 mmol) was dissolved in ethyl acetate (14 mL), and 10% palladium-carbon catalyst (containing 50% water, 320 mg) was added. The reaction was stirred at 20-25°C for 3 hours under hydrogen atmosphere (0.25 MPa). Upon completion of the reaction, the palladium-carbon catalyst was removed by filtration and the solvent was removed by distillation under reduced pressure. The resulting crude product was purified by silica gel column chromatography with hexane/ethyl acetate (10:1 to 5:1) as eluent to afford methyl 2-amino-5-methoxybenzoate (1.29 g, 94% yield). The product was characterized by 1H-NMR (CDCl3), δ: 3.76 (3H, s), 3.88 (3H, s), 5.37 (2H, br), 6.63 (1H, d, J = 8.8 Hz), 6.95 (1H, dd, J = 8.8, 3.1 Hz), 7.35 (1H, d, J = 3.1 Hz).

[References]

[1] Patent: EP1724268, 2006, A1. Location in patent: Page/Page column 50
[2] Synlett, 2016, vol. 27, # 8, p. 1237 - 1240
[3] Patent: EP1844768, 2007, A1. Location in patent: Page/Page column 25
[4] Patent: CN106478548, 2017, A. Location in patent: Paragraph 0089; 0090; 0121; 0122; 0137; 0138
[5] Australian Journal of Chemistry, 1972, vol. 25, p. 2621 - 2629
Spectrum DetailBack Directory
[Spectrum Detail]

METHYL 2-AMINO-5-METHOXYBENZOATE(2475-80-1)1HNMR
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