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2-(2'-BROMOPHENOXY)PROPANE

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2-(2'-BROMOPHENOXY)PROPANE Basic information

Product Name:
2-(2'-BROMOPHENOXY)PROPANE
Synonyms:
  • 1-bromo-2-propan-2-yloxybenzene
  • 1-Bromo-2-isopropoxybenzen
  • 2-BROMOISOPROPOXYBENZENE
  • 2-(2'-BROMOPHENOXY)PROPANE
  • O-BROMOISOPROPOXYBENZENE
  • 1-Bromo-2-isopropoxybenzene
  • 1-Bromo-2-isopropoxybenzene >
  • Benzene, 1-bromo-2-(1-methylethoxy)-
CAS:
701-07-5
MF:
C9H11BrO
MW:
215.09
Product Categories:
  • Anisoles, Alkyloxy Compounds & Phenylacetates
  • Bromine Compounds
Mol File:
701-07-5.mol
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2-(2'-BROMOPHENOXY)PROPANE Chemical Properties

Boiling point:
73 °C / 2mmHg
Density 
1.34
refractive index 
1.5360-1.5400
storage temp. 
Sealed in dry,Room Temperature
form 
clear liquid
color 
Colorless to Light yellow
Water Solubility 
Slightly soluble in water.
CAS DataBase Reference
701-07-5(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36/37/39
HS Code 
2909309090
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2-(2'-BROMOPHENOXY)PROPANE Usage And Synthesis

Chemical Properties

Colorless liquid

Uses

1-Bromo-2-isopropoxybenzene is used as an intermediate in organic syntheses.

Synthesis

95-56-7

75-26-3

701-07-5

General procedure for the synthesis of 1-bromo-2-isopropoxybenzene from 2-bromophenol and 2-bromopropane: A mixture of 2-bromophenol (1.156 mmol), anhydrous K2CO3 (1.20 eq., 192 mg), sodium iodide (4 mg), and anhydrous ethanol (3 mL) was magnetically stirred at room temperature under argon protection. 2-Bromopropane (1.20 eq.) was added slowly and the mixture was then refluxed for 5 hours. After the reaction was complete, it was cooled to room temperature and the solvent was removed under reduced pressure. Ethyl acetate (50 mL) was added to dissolve the residue and the organic phase was washed sequentially with 1M NaOH and brine (15 mL each). The organic phase was dried with anhydrous Na2SO4 and the solvent was evaporated under reduced pressure to obtain the crude product. Finally, the crude product was purified by fast column chromatography.

References

[1] Journal of Organic Chemistry, 2000, vol. 65, # 26, p. 9143 - 9151
[2] Journal of Medicinal Chemistry, 1998, vol. 41, # 12, p. 1997 - 2009
[3] Organic Preparations and Procedures International, 2015, vol. 47, # 3, p. 227 - 231
[4] Patent: WO2009/55674, 2009, A1. Location in patent: Page/Page column 59
[5] Journal of Medicinal Chemistry, 2012, vol. 55, # 9, p. 4189 - 4204

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