Basic information Safety Supplier Related

1-(2-Bromoethyl)-4-(trifluoromethyl)benzene, 2-(4-Trifluoromethylphenyl)ethyl bromide

Basic information Safety Supplier Related

1-(2-Bromoethyl)-4-(trifluoromethyl)benzene, 2-(4-Trifluoromethylphenyl)ethyl bromide Basic information

Product Name:
1-(2-Bromoethyl)-4-(trifluoromethyl)benzene, 2-(4-Trifluoromethylphenyl)ethyl bromide
Synonyms:
  • 1-(2-Bromoethyl)-4-(trifluoromethyl)benzene, 2-(4-Trifluoromethylphenyl)ethyl bromide
  • 2-(4-trifluoromethylphenyl)ethyl bromide
  • 4-(Trifluoromethyl)phenethyl bromide
  • 4-TrifluoroMethylphenyl)ethyl broMide
  • 1-(2-broMoethyl)-4-(trifluoroMethyl)benzene
  • 4-(TrifluoroMethyl)phenethyl broMide 97%
  • Benzene, 1-(2-bromoethyl)-4-(trifluoromethyl)-
CAS:
130365-87-6
MF:
C9H8BrF3
MW:
253.06
Mol File:
130365-87-6.mol
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1-(2-Bromoethyl)-4-(trifluoromethyl)benzene, 2-(4-Trifluoromethylphenyl)ethyl bromide Chemical Properties

Boiling point:
218.0±35.0 °C(Predicted)
Density 
1.499 g/mL at 25 °C
refractive index 
n20/D 1.487
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
form 
liquid
Appearance
Colorless to light yellow Liquid
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Safety Information

Hazard Codes 
Xn,N
Risk Statements 
22-36-51/53
Safety Statements 
26-61
RIDADR 
UN 3082 9/PG 3
WGK Germany 
3
HS Code 
2903998090
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1-(2-Bromoethyl)-4-(trifluoromethyl)benzene, 2-(4-Trifluoromethylphenyl)ethyl bromide Usage And Synthesis

Synthesis

2968-93-6

130365-87-6

Step ii: Synthesis of 1-(2-bromoethyl)-4-(trifluoromethyl)benzene To a 50 mL round bottom flask was added 2-(4-(trifluoromethyl)phenyl)ethanol (7.9 g, 0.0415 mol) and phosphorus tribromide (5.6 g, 0.0207 mol). The reaction mixture was stirred at 100 °C for 2 hours. After completion of the reaction, the reaction was quenched by adding ice-cold water to the mixture. The reaction mixture was extracted with hexane and the organic layer was separated. The organic layer was washed with brine and dried over anhydrous sodium sulfate. The solvent was removed by concentration under reduced pressure to give the crude product. The crude product was purified by column chromatography using 60-120 mesh silica gel as stationary phase and 0-5% ethyl acetate in hexane solution as eluent to give 4-(trifluoromethyl)phenylethyl bromide (7.8 g, 74% yield). 1H NMR (300 MHz, CDCl3): δ 7.60 (d, 2H), 7.35 (d, 2H), 3.61 (t, 2H), 3.25 (t, 2H).

References

[1] Patent: WO2015/101928, 2015, A1. Location in patent: Page/Page column 127;
[2] Patent: WO2005/123748, 2005, A1. Location in patent: Page/Page column 97-98
[3] Patent: WO2005/49613, 2005, A1. Location in patent: Page/Page column 48-49
[4] Patent: WO2007/69986, 2007, A1. Location in patent: Page/Page column 87

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