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2-AMino-4-broMo-5-fluorophenol

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2-AMino-4-broMo-5-fluorophenol Basic information

Product Name:
2-AMino-4-broMo-5-fluorophenol
Synonyms:
  • 5-Bromo-4-fluoro-2-hydroxyaniline
  • Phenol, 2-amino-4-bromo-5-fluoro-
  • 2-AMino-4-broMo-5-fluorophenol ISO 9001:2015 REACH
CAS:
1016234-89-1
MF:
C6H5BrFNO
MW:
206.01
Mol File:
1016234-89-1.mol
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2-AMino-4-broMo-5-fluorophenol Chemical Properties

Boiling point:
288.7±40.0 °C(Predicted)
Density 
1.863±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
pka
8.21±0.23(Predicted)
form 
powder
color 
Dark brown
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Safety Information

HS Code 
2922290090
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2-AMino-4-broMo-5-fluorophenol Usage And Synthesis

Synthesis

1016234-87-9

1016234-89-1

GENERAL STEPS: A suspension of sodium conodisulfite (Na2S2O4, 51.6 g, 296 mmol) in water (122 mL) was slowly added to a refluxed solution of 4-bromo-5-fluoro-2-nitrophenol (14 g, 59.3 mmol) in ethanol (1000 mL). The reaction mixture was continued to reflux for 1 hour. After completion of the reaction, it was cooled to room temperature and filtered to remove the resulting salt. The filtrate was partially concentrated and subsequently saturated aqueous sodium chloride solution was added and extracted with ether. The organic phases were combined, dried with anhydrous sodium sulfate and concentrated under reduced pressure to afford the crude 2-amino-4-bromo-5-fluorophenol (9.2 g, 75% yield), which was used in the subsequent reaction without further purification.1H-NMR (400 MHz, DMSO-d6) δ: 4.65 (br s, 2H, NH2), 6.60 (d, J = 11.3 Hz, 1H ArH), 6.76 (d, J = 7.8 Hz, 1H, ArH), 9.80 (br s, 1H, OH).

References

[1] Patent: WO2008/37746, 2008, A1. Location in patent: Page/Page column 15
[2] Patent: US2008/90804, 2008, A1. Location in patent: Page/Page column 7
[3] Patent: WO2008/37746, 2008, A1. Location in patent: Page/Page column 15
[4] Patent: WO2010/130773, 2010, A2. Location in patent: Page/Page column 66

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