Basic information Safety Supplier Related

Ethyl 4-amino-3-methoxybenzoate

Basic information Safety Supplier Related

Ethyl 4-amino-3-methoxybenzoate Basic information

Product Name:
Ethyl 4-amino-3-methoxybenzoate
Synonyms:
  • Ethyl 3-methoxy-4-aminobenzoate
  • Ethyl 4-amino-3-methoxybenzoate
  • Benzoic acid, 4-amino-3-methoxy-, ethyl ester
  • Ethyl 4-amino-3-methoxybenzoate 13C6
  • Benzoic acid, 4-amino-3-methoxy-, ethyl ester (9CI, ACI)
  • 4-amino-3-methoxy-Benzoic acid ethyl ester (9CI ACI)
CAS:
73368-41-9
MF:
C10H13NO3
MW:
195.22
Product Categories:
  • Acids & Esters
  • Anisoles, Alkyloxy Compounds & Phenylacetates
  • Iodine Compounds
Mol File:
73368-41-9.mol
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Ethyl 4-amino-3-methoxybenzoate Chemical Properties

Melting point:
84-85 °C
Boiling point:
343.6±22.0 °C(Predicted)
Density 
1.147±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
pka
2.45±0.10(Predicted)
Appearance
White to off-white Solid
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Ethyl 4-amino-3-methoxybenzoate Usage And Synthesis

Synthesis

64-17-5

2486-69-3

73368-41-9

A 22-liter three-necked round-bottom flask (RBF) was assembled with an electric heating jacket, thermocouple probe, overhead mechanical stirrer, water-cooled condenser, nitrogen bubbler, and charging funnel. 4-Amino-3-methoxybenzoic acid (1.0 kg, 5.98 mol, 1.0 eq.) and ethanol (10.0 l, 10 v/v) were added to the flask to form a stir-able slurry. Sulfuric acid (1.17 kg, 0.64 L, 12.0 mol, 2.0 eq.) was slowly added for 1 hour without external cooling. The slurry initially thickened, then dispersed and eventually dissolved completely to form a dark solution. Exotherm during spiking raised the temperature to 45 °C; additional heat was then applied to reflux the solution and it was kept refluxing overnight. Analysis by HPLC sampling showed 5% of the starting benzoic acid remaining. The condenser was switched to distillation mode and 2.5 liters of solvent was distilled. The reaction mixture was cooled to 6 °C in an ice bath and the pH was adjusted to 12 by slow addition of aqueous sodium hydroxide (50 wt%, 1.03 kg, 681 mL, 12.9 mol, 2.15 eq.), controlling the temperature to be below 20 °C. After stirring for 30 minutes, an additional amount of water (4.0 liters) was added and stirring was continued for 30 minutes at about 10°C. The solid product was collected by filtration, washed thoroughly with water (4.0 liters) and subsequently dried under vacuum at 65 °C overnight. Ethyl 4-amino-3-methoxybenzoate 1.04 kg (89.1% yield) was obtained as a light brown solid. Melting point: 83-87 °C (DSC measurement); 1H NMR (300 MHz, CDCl3) δ 7.56 (1H, dd, J = 7.9,1.5 Hz), 7.47 (1H, d, J = 1.5 Hz), 6.66 (1H, d, J = 7.9 Hz), 4.33 (2H, t, J = 7.2 Hz), 4.27 (1H, br s) , 3.90 (3H, s), 1.37 (3H, t, J = 7.2 Hz).

References

[1] Journal of the American Chemical Society, 1998, vol. 120, # 14, p. 3332 - 3339
[2] Patent: WO2014/128094, 2014, A1. Location in patent: Page/Page column 22
[3] European Journal of Medicinal Chemistry, 2007, vol. 42, # 5, p. 567 - 579
[4] Patent: US2009/259049, 2009, A1. Location in patent: Page/Page column 12
[5] Patent: US2011/86882, 2011, A1. Location in patent: Page/Page column 27

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