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3',4',5'-TRIFLUOROACETOPHENONE

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3',4',5'-TRIFLUOROACETOPHENONE Basic information

Product Name:
3',4',5'-TRIFLUOROACETOPHENONE
Synonyms:
  • 3,4,5-TRIFLUOROACETOPHENONE
  • 3',4',5'-Trifluoroacetophenone 97%
  • 3',4',5'-Trifluoroacetophenone97%
  • 1-(3,4,5-trifluorophenyl)ethanone
  • 1-(3,4,5-Trifluorophenyl)ethan-1-one
  • Ethanone, 1-(3,4,5-trifluorophenyl)-
  • 3',4',5'-Trifluoroacetophenone
  • 3',4',5'-TRIFLUOROACETOPHE
CAS:
220141-73-1
MF:
C8H5F3O
MW:
174.12
EINECS:
671-898-5
Product Categories:
  • Fluorine series
  • ketone
Mol File:
220141-73-1.mol
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3',4',5'-TRIFLUOROACETOPHENONE Chemical Properties

Boiling point:
209℃
Density 
1.303
refractive index 
1.473
Flash point:
>100°C
storage temp. 
Sealed in dry,Room Temperature
form 
clear liquid
color 
Colorless to Light yellow
CAS DataBase Reference
220141-73-1(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi,F
Risk Statements 
36/37/38
Safety Statements 
26-36
RIDADR 
1993
Hazard Note 
Irritant/Flammable
HazardClass 
IRRITANT
HS Code 
2914790090

MSDS

  • Language:English Provider:ALFA
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3',4',5'-TRIFLUOROACETOPHENONE Usage And Synthesis

Chemical Properties

colorless to clear liquid

Uses

3',4',5'-Trifluoroacetophenone is an organic intermediate that can be used to prepare the key mother nucleus (S)-N-[4-(1-aminoethyl)-2,6-difluorophenyl]methanesulfonamide of vanilloid compounds.

Synthesis

108-24-7

138526-69-9

220141-73-1

The general procedure for the synthesis of 3,4,5-trifluoroacetophenone from ethanoic anhydride and 3,4,5-trifluorobromobenzene was carried out as follows: firstly, iodine (361 mg, 1.42 mmol) was added to a solution of magnesium (3.53 g, 145 mmol) in tetrahydrofuran (100 ml) at room temperature, followed by slow dropwise addition of 3,4,5-trifluorobromobenzene (30.0 g, 142 mmol). The reaction mixture was stirred at the same temperature for 30 minutes. Next, a toluene solution (100 ml) containing copper (I) chloride (704 mg, 7.11 mmol) and acetic anhydride (16.0 g, 156 mmol) was added to the reaction mixture at 0°C. The reaction mixture was continued to be stirred at 0°C for 1 hour. After completion of the reaction, the mixture was poured into 2N aqueous hydrochloric acid solution and extracted with toluene. The extract was washed with saturated brine, dried over anhydrous sodium sulfate and subsequently concentrated under reduced pressure. The concentrated product was purified by silica gel column chromatography using ethyl acetate/hexane (1/10) as elution solvent to give 3,4,5-trifluoroacetophenone as a final yellow oil (yield 21.0 g, 85% yield).

References

[1] Patent: JP2016/84346, 2016, A. Location in patent: Paragraph 0056
[2] Patent: JP2016/84328, 2016, A. Location in patent: Paragraph 0191

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