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4-Bromo-2-chlorobenzotrifluoride

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4-Bromo-2-chlorobenzotrifluoride Basic information

Product Name:
4-Bromo-2-chlorobenzotrifluoride
Synonyms:
  • 4-bromo-2-chloro-1-(trifluoromethyl)benzene
  • 4-Bromo-2-chlorobenzotrifluoride
  • 4-Bromo-2-chloro-1-(trifluoromethyl)benzene 4-Bromo-2-chloro-alpha,alpha,alpha-trifluorotoluene
  • Benzene,4-broMo-2-chloro-1-(trifluoroMethyl)-
  • 2-chloro-4-bromotrifluorotoluene
  • 2-chloro-4-bromo-trifluoromethylbenzene
  • 2-Chloride-4-Bromine Benzotrifluoride
  • 4-Bromo-2-chlorobenzotrifluoride >
CAS:
467435-07-0
MF:
C7H3BrClF3
MW:
259.45
Product Categories:
  • Trifluoromethyl-benzene series
Mol File:
467435-07-0.mol
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4-Bromo-2-chlorobenzotrifluoride Chemical Properties

Boiling point:
224.1±35.0 °C(Predicted)
Density 
1.76
refractive index 
1.5040-1.5080
storage temp. 
Sealed in dry,Room Temperature
form 
clear liquid
color 
Colorless to Almost colorless
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Safety Information

Hazard Codes 
Xi
HazardClass 
IRRITANT, IRRITANT-HARMFUL
HS Code 
2903998090
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4-Bromo-2-chlorobenzotrifluoride Usage And Synthesis

Chemical Properties

Colorless liquid

Synthesis

445-13-6

467435-07-0

The general procedure for the synthesis of 4-bromo-2-chlorobenzotrifluoride using 4-amino-2-chlorobenzotrifluoride as starting material was as follows: 4-amino-2-chlorobenzotrifluoride (9.780 g; 50.007 mmol) was dissolved in acetonitrile (65 mL), and copper(II) bromide (11.169 g; 50.007 mmol) was added to form a green, non-homogeneous mixture. The mixture was heated to 45°C. Subsequently, a solution of tert-butyl nitrite (6.53 mL; 55.008 mmol) in acetonitrile (10 mL) was added slowly and dropwise over 30 minutes. After the dropwise addition, the reaction mixture was continued to be stirred at 45°C for 2 hours. Upon completion of the reaction, the dark, inhomogeneous mixture was cooled to room temperature and purified directly by fast column chromatography (dichloromethane as eluent). After concentration under reduced pressure to remove the solvent, the target product, 4-bromo-2-chloro-1-trifluoromethylbenzene, was obtained as a yellow oil (12.820 g; 50% yield).LC-MS analysis: retention time t R = 1.10 min; [M + H]+: no ionization peak was observed.

References

[1] Patent: WO2008/78291, 2008, A1. Location in patent: Page/Page column 42

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