Identification | More | [Name]
2-(4-CHLOROPHENOXY)ANILINE | [CAS]
2770-11-8 | [Synonyms]
2-(4'-CHLOROPHENOXY)ANILINE 2-(4-CHLOROPHENOXY)ANILINE 2-AMINO-4'-CHLORODIPHENYL ETHER 2-(4-chlorophenoxy)benzenamine | [EINECS(EC#)]
220-461-3 | [Molecular Formula]
C12H10ClNO | [MDL Number]
MFCD00025168 | [Molecular Weight]
219.67 | [MOL File]
2770-11-8.mol |
Chemical Properties | Back Directory | [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) |
Hazard Information | Back Directory | [Chemical Properties]
pale yellow powder | [Uses]
Amoxapine impurity. | [Synthesis]
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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