Basic information Safety Supplier Related

4-Bromo-1-difluoromethoxy-2-methyl-benzene

Basic information Safety Supplier Related

4-Bromo-1-difluoromethoxy-2-methyl-benzene Basic information

Product Name:
4-Bromo-1-difluoromethoxy-2-methyl-benzene
Synonyms:
  • 4-Bromo-1-difluoromethoxy-2-methyl-benzene
  • 1-Bromo-3-methyl-4-(difluoromethoxy)benzene
  • 5-Bromo-2-(difluoromethoxy)toluene
  • 4-BroMo-2-Methy-1-(difluoroMethoxy)benzene
  • Benzene, 4-bromo-1-(difluoromethoxy)-2-methyl-
CAS:
888327-32-0
MF:
C8H7BrF2O
MW:
237.04
Product Categories:
  • Fluorine series
Mol File:
888327-32-0.mol
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4-Bromo-1-difluoromethoxy-2-methyl-benzene Chemical Properties

Boiling point:
223℃
Density 
1.508
Flash point:
108℃
storage temp. 
Sealed in dry,Room Temperature
form 
liquid
color 
Colourless
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Safety Information

HS Code 
2909309090
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4-Bromo-1-difluoromethoxy-2-methyl-benzene Usage And Synthesis

Synthesis

83190-02-7

888327-32-0

General procedure for the synthesis of 5-bromo-2-(difluoromethoxy)toluene from 4-(difluoromethoxy)-3-methylaniline: to a stirred solution of 4-amino-1-(difluoromethoxy)-2-methylbenzene (5 g, 28.90 mmol) in a mixture of hydrobromic acid (20 mL) and water (20 mL), at 0 °C, sodium nitrite (2.07 g 30.00 mmol) in aqueous solution (10 mL), and the titration process was controlled to be completed within 20 minutes. After the dropwise addition, the reaction mixture was continued to be stirred at 0 °C for 30 min. Subsequently, copper (I) bromide (4 g, 27.87 mmol) was added and the mixture was heated to 60 °C for 30 min of reaction. Upon completion of the reaction, the reaction mixture was extracted with ethyl acetate (3 x 50 mL), the organic layers were combined, washed once with water (10 mL), dried over anhydrous sodium sulfate and concentrated to give 2.5 g of 4-bromo-1-(difluoromethoxy)-2-methylbenzene in 37% yield.

References

[1] Patent: WO2006/55187, 2006, A1. Location in patent: Page/Page column 83

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