Basic information Safety Supplier Related

4-AMINO-3-BROMO-BENZOIC ACID ETHYL ESTER

Basic information Safety Supplier Related

4-AMINO-3-BROMO-BENZOIC ACID ETHYL ESTER Basic information

Product Name:
4-AMINO-3-BROMO-BENZOIC ACID ETHYL ESTER
Synonyms:
  • 4-AMINO-3-BROMO-BENZOIC ACID ETHYL ESTER
  • ETHYL 4-AMINO-3-BROMOBENZOATE
  • BUTTPARK 41\01-29
  • Ethyl-3-broMo-4-aMino benzoate
  • NSC 51689
  • Benzoic acid, 4-amino-3-bromo-, ethyl ester
CAS:
7149-03-3
MF:
C9H10BrNO2
MW:
244.09
Product Categories:
  • Acids & Esters
  • Anilines, Amides & Amines
  • Bromine Compounds
  • pharmacetical
Mol File:
7149-03-3.mol
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4-AMINO-3-BROMO-BENZOIC ACID ETHYL ESTER Chemical Properties

Melting point:
90-92 °C
Boiling point:
345.2±22.0 °C(Predicted)
Density 
1.503±0.06 g/cm3(Predicted)
storage temp. 
2-8°C(protect from light)
pka
0.44±0.10(Predicted)
Appearance
White to off-white Solid
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Safety Information

HS Code 
2922498590
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4-AMINO-3-BROMO-BENZOIC ACID ETHYL ESTER Usage And Synthesis

Synthesis

94-09-7

7149-03-3

General procedure for the synthesis of ethyl 3-bromo-4-aminobenzoate from ethyl 4-aminobenzoate: ethyl 4-aminobenzoate (10 g, 61 mmol) was dissolved in DMF (150 mL) under cooling conditions in an ice bath. Subsequently, N-bromosuccinimide (NBS, 10.8 g, 61 mmol) was added in batches and stirred continuously at the same temperature for 30 min. Upon completion of the reaction, the ice bath was removed and the reaction mixture was allowed to continue stirring at room temperature overnight (~18 hours). The reaction mixture was poured into water (500 mL) and the precipitate was collected by filtration. The resulting orange solid was washed with water (50 mL x 2) and recrystallized by ethanol to give the light yellow crystalline product ethyl 3-bromo-4-aminobenzoate (13.3 g, 91% yield). The product was detected by thin layer chromatography (TLC) with an Rf value of 0.38 (Expander ratio: petroleum ether:ethyl acetate=5:1). The melting point was 86-88°C. 1H-NMR (CDCl3, 300MHz) δ: 8.07 (s, 1H), 7.79 (t, J = 11.55Hz, 1H), 6.70 (d, J = 8.10Hz, 1H), 4.58 (br, 2H), 4.37 (dd, J = 6.6Hz, J = 6.6Hz, 2H), 1.34 ( t, J = 7.2 Hz, 3H).

References

[1] Journal of the American Chemical Society, 2002, vol. 124, # 19, p. 5350 - 5364
[2] European Journal of Organic Chemistry, 2010, # 24, p. 4662 - 4670
[3] Tetrahedron Letters, 2012, vol. 53, # 39, p. 5248 - 5252
[4] Patent: US2005/282825, 2005, A1. Location in patent: Page/Page column 8
[5] Journal of Medicinal Chemistry, 2012, vol. 55, # 17, p. 7360 - 7377

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