Basic information Safety Supplier Related

2-bromo-6-methoxy-aniline

Basic information Safety Supplier Related

2-bromo-6-methoxy-aniline Basic information

Product Name:
2-bromo-6-methoxy-aniline
Synonyms:
  • 2-Bromo-6-methoxyaniline97%
  • 2-Amino-3-bromoanisole
  • Nsc29554
  • 2-Bromo-6-methoxyaniline 97%
  • 2-Amino-3-bromoanisole, 6-Bromo-o-anisidine
  • BenzenaMine, 2-broMo-6-Methoxy-
  • 2-BroMo-6-Methoxy-phenylaMine
CAS:
5473-01-8
MF:
C7H8BrNO
MW:
202.05
Mol File:
5473-01-8.mol
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2-bromo-6-methoxy-aniline Chemical Properties

Boiling point:
251.3±20.0 °C(Predicted)
Density 
1.531±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
pka
2.48±0.10(Predicted)
form 
liquid
color 
Yellow
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Safety Information

HS Code 
2922290090
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2-bromo-6-methoxy-aniline Usage And Synthesis

Synthesis

90-04-0

5473-01-8

Step A: Synthesis of 6-bromo-2-anisidine. A solution of bromine (1.22 mL, 23.7 mmol) in acetic acid (10 mL) was slowly added dropwise to a cooled solution of o-methoxyaniline (2.7 mL, 23.7 mmol) in hexadecanecarboxylic acid (20 mL) for a controlled time period of 10 minutes at 10°C. The reaction mixture was then stirred for 10 minutes. After the dropwise addition was completed, the reaction mixture was continued to be stirred for 10 min. Upon completion of the reaction, the solvent was removed by rotary evaporation and the residue was dissolved in ethyl acetate. The solution was sequentially washed with saturated sodium bicarbonate solution and dried with anhydrous magnesium sulfate. After drying, the desiccant was removed by filtration and the filtrate was concentrated by rotary evaporation. The crude product was purified by fast column chromatography on silica gel, the eluent being a hexane solution of 45% dichloromethane, resulting in 3.44 g of 2-bromo-6-methoxyaniline in 72% yield.

References

[1] Patent: US6291511, 2001, B1

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