Basic information Safety Supplier Related

2-(4-CHLOROPHENOXY)ANILINE

Basic information Safety Supplier Related

2-(4-CHLOROPHENOXY)ANILINE Basic information

Product Name:
2-(4-CHLOROPHENOXY)ANILINE
Synonyms:
  • 2-(4'-CHLOROPHENOXY)ANILINE
  • 2-(4-CHLOROPHENOXY)ANILINE
  • 2-(4-chlorophenoxy)benzenamine
  • [2-(4-chlorophenoxy)phenyl]amine
  • 2-Amino-4'-chlorodiphenyl Ether >
  • Amoxapine Impurity 2
  • Benzenamine, 2-(4-chlorophenoxy)-
  • Amoxapine RC 4
CAS:
2770-11-8
MF:
C12H10ClNO
MW:
219.67
EINECS:
220-461-3
Product Categories:
  • Amines
  • Impurities
  • Intermediates
  • Intermediates & Fine Chemicals
  • Pharmaceuticals
Mol File:
2770-11-8.mol
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2-(4-CHLOROPHENOXY)ANILINE Chemical Properties

Boiling point:
202°C/15mmHg(lit.)
Density 
1.260±0.06 g/cm3(Predicted)
refractive index 
1.6180-1.6220
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
solubility 
Chloroform (Sparingly), Methanol (Slightly)
form 
Oil
pka
3.69±0.10(Predicted)
color 
Colourless to Light Orange
CAS DataBase Reference
2770-11-8(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
HazardClass 
IRRITANT
HS Code 
2922290090
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2-(4-CHLOROPHENOXY)ANILINE Usage And Synthesis

Chemical Properties

pale yellow powder

Uses

Amoxapine impurity.

Synthesis

39145-47-6

2770-11-8

General procedure for the synthesis of 4'-chloro-2-amino-diphenyl ether from 1-(4-chlorophenoxy)-2-nitrobenzene: A mixture of commercially available iron powder (3.18 g, 57.28 mmol) and ammonium chloride (383 mg, 7.15 mmol) in ethanol (45 mL) and water (8 mL) was refluxed. To this mixture was added 1-(4-chlorophenoxy)-2-nitrobenzene (AMR01028,2.2 g, 8.81 mmol) and the resulting mixture was stirred at reflux for 1 hour. After completion of the reaction, the solvent was removed and the residue was diluted in aqueous sodium bicarbonate (40 mL) and extracted with dichloromethane (3 x 20 mL). The organic layers were combined, dried with anhydrous magnesium sulfate, filtered and the solvent was evaporated to give 4'-chloro-2-amino-diphenyl ether (AMR01029,1.50 g, 78%) as a colorless oil, which could be used in the next step without further purification. Thin layer chromatography (TLC) Rf value was 0.53 (unfolding agent: dichloromethane).1H NMR (270MHz, CDCl3) data: δ 3.77 (2H, broad single peak, NH2), 6.71 (1H, multiple peaks), 6.83 (2H, multiple peaks), 6.89 (2H, AA'BB' system), 6.99 (1H, multiple peaks), 7.25 ( 2H, AA'BB' system).

References

[1] Patent: WO2007/3934, 2007, A2. Location in patent: Page/Page column 119
[2] Journal of the American Chemical Society, 2014, vol. 136, # 40, p. 14060 - 14067
[3] Journal of the Chemical Society, 1931, p. 529,533
[4] Journal of the Chemical Society, 1925, vol. 127, p. 2011
[5] Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1976, p. 1279 - 1285

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