Basic information Safety Supplier Related

4-(TRIFLUOROACETYL)TOLUENE

Basic information Safety Supplier Related

4-(TRIFLUOROACETYL)TOLUENE Basic information

Product Name:
4-(TRIFLUOROACETYL)TOLUENE
Synonyms:
  • (Trifluoromethyl)-p-tolylketone
  • Ethanone,2,2,2-trifluoro-1-(4-methylphenyl)-
  • 4-(TRIFLUOROACETYL)TOLUENE
  • 2,2,2-TRIFLUORO-1-(P-TOLYL)ETHANONE
  • 4-(Trifluoroacetyl)toluene97.
  • 4'-Methyl-2,2,2-trifluoroacetophenone 97%
  • 4'-Methyl-2,2,2-trifluoroacetophenone 4-(Trifluoroacetyl)toluene
  • 4-(Trifluoroacetyl)toluene, 1-(4-Methylphenyl)-2,2,2-trifluoroethan-1-one
CAS:
394-59-2
MF:
C9H7F3O
MW:
188.15
Mol File:
394-59-2.mol
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4-(TRIFLUOROACETYL)TOLUENE Chemical Properties

Melting point:
5°C
Boiling point:
70 °C
Density 
1.2304 g/cm3(Temp: 25 °C)
refractive index 
1.47
Flash point:
70-72°C/15mm
storage temp. 
Sealed in dry,Room Temperature
solubility 
Chloroform (Slightly), Ethyl Acetate (Slightly), Methanol (Slightly)
form 
clear liquid
color 
Colorless to Light yellow to Light orange
BRN 
1870406
CAS DataBase Reference
394-59-2(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36/37/39-37
HazardClass 
IRRITANT
HS Code 
29039990

MSDS

  • Language:English Provider:ALFA
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4-(TRIFLUOROACETYL)TOLUENE Usage And Synthesis

Chemical Properties

Clear colorless to light yellow liquid

Uses

p-Trifluoroacetyltoluene is used as a reagent in the synthesis of 5-methylene-2-(trifluoromethyl)morpholin-3-one derivatives which have fungicidal activity.

Synthesis

In a nitrogen atmosphere, one PTFE magnet was placed in a reactor, and 0.4 mmol p-methylbenzene diazonium tetrafluoroborate, 0.1 mmol cuprous oxide, 1 , 0.8 mmol dimethyl sulfoxide, and finally 1.2 mmol ethyl trifluoropyruvate were added. mL of dichloromethane, 0.8 mmol of dimethyl sulfoxide, and finally 1.2 mmol of ethyl trifluoropyruvate were added, and the reaction was stirred at 25 ??C for 16 in a closed system. After h, the reaction was extracted with ether 3 times, 10 mL each time, the organic phases were combined and washed with distilled water 3 times, the organic phase was dried with anhydrous magnesium sulfate, filtered, and then rotary evaporated to remove the organic solvent . The obtained crude product was eluted by silica gel column chromatography with n-pentane as eluent to obtain 4-(trifluoroacetyl)toluene (86% isolated yield).

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