2-(4-CHLOROPHENOXY)ANILINE
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
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)
Safety Information
- Hazard Codes
- Xi
- HazardClass
- IRRITANT
- HS Code
- 2922290090
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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2-(4-CHLOROPHENOXY)ANILINE(2770-11-8)Related Product Information
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- Loxapine succinate salt
- 2-(4-CHLOROPHENOXY)ANILINE
- 4-(4-CHLORO-3-METHYLPHENOXY)-3-NITROBENZOTRIFLUORIDE
- 2-(2,4-DICHLOROPHENOXY)ANILINE HYDROCHLORIDE
- 5-chloro-2-(2,4-dichlorophenoxy)aniline
- 2-(2,4-Dichlorophenoxy)aniline
- 1-[(4-Chlorophenyl)oxy]-2-nitrobenzene
- 4-Chloro-1-(4-chlorophenoxy)-2-nitrobenzene
- 2,4-DICHLORO-4'-AMINODIPHENYL ETHER
- 4-Amino-4'-chlorodiphenyl ether
- 2-(2-CHLOROPHENOXY)ANILINE
- 5-Chloro-2-(2-chlorophenoxy)aniline
- 2-(3-CHLOROPHENOXY)ANILINE
- 3-CHLORO-2-(3-CHLOROPHENOXY)ANILINE
- 4-Chlorodiphenyl ether
- Aniline
- 2-AMINO-4'-CHLORO-4-TRIFLUOROMETHYL DIPHENYL ETHER