Basic information Safety Supplier Related

1-(2-BROMOETHOXY)-4-FLUOROBENZENE

Basic information Safety Supplier Related

1-(2-BROMOETHOXY)-4-FLUOROBENZENE Basic information

Product Name:
1-(2-BROMOETHOXY)-4-FLUOROBENZENE
Synonyms:
  • ASISCHEM Z95334
  • AKOS BC-2656
  • 4-FLUOROPHENOXY-ETHYLBROMIDE
  • 4-(2-BROMOETHOXY)FLUOROBENZENE
  • 2-(4-FLUOROPHENOXY)ETHYL BROMIDE
  • 1-BROMO-2-(4'-FLUOROPHENOXY)ETHANE
  • 1-(2-BROMOETHOXY)-4-FLUOROBENZENE
  • (P-FLUOROPHENOXY)ETHYLBROMIDE
CAS:
332-48-9
MF:
C8H8BrFO
MW:
219.05
Product Categories:
  • Anisoles, Alkyloxy Compounds & Phenylacetates
  • Bromine Compounds
  • Fluorine Compounds
Mol File:
332-48-9.mol
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1-(2-BROMOETHOXY)-4-FLUOROBENZENE Chemical Properties

Melting point:
58-60 °C
Boiling point:
66°C/0.1mmHg(lit.)
Density 
1.4901 (rough estimate)
refractive index 
1.53-1.532
storage temp. 
Storage temp. 2-8°C
form 
Liquid After Melting
color 
Clear colorless to brownish
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Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
36/37/38-52-22
Safety Statements 
24/25
HazardClass 
IRRITANT
HS Code 
29093090

MSDS

  • Language:English Provider:ACROS
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1-(2-BROMOETHOXY)-4-FLUOROBENZENE Usage And Synthesis

Chemical Properties

clear colorless to brownish liquid after melting

Synthesis

371-41-5

106-93-4

332-48-9

Step 2: 22.5% aqueous sodium hydroxide solution (55 mL) was slowly added to a mixed reaction flask containing 1,2-dibromoethane (112 g, 0.60 mol) and 4-fluorophenol (16.8 g, 0.15 mol). The reaction mixture was heated and stirred under reflux conditions for 5 hours. Subsequently, sodium hydroxide (3.0 g, 75 mmol) was added to the reaction system and heating and stirring were continued under reflux conditions for 5 hours. After completion of the reaction, the reaction solution was cooled to room temperature and extracted three times with dichloromethane (100 mL). The organic layers were combined, dried with anhydrous sodium sulfate and the solvent was removed by distillation under reduced pressure. The resulting crude product was purified by silica gel column chromatography (eluent: petroleum ether/ethyl acetate=10:1, v/v) to afford 1-(2-bromoethoxy)-4-fluorobenzene (compound-03) (29.7 g, 0.136 mol, 90% yield).

References

[1] Patent: EP2357165, 2011, A1. Location in patent: Page/Page column 18
[2] Bioorganic and Medicinal Chemistry Letters, 2001, vol. 11, # 4, p. 495 - 500
[3] Russian Journal of Organic Chemistry, 2000, vol. 36, # 2, p. 254 - 257
[4] Archiv der Pharmazie, 2013, vol. 346, # 3, p. 180 - 188
[5] European Journal of Medicinal Chemistry, 1992, vol. 27, # 5, p. 545 - 549

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