Basic information Safety Supplier Related

ETHYL 4-(TRIFLUOROMETHYL)PHENYL ACETATE

Basic information Safety Supplier Related

ETHYL 4-(TRIFLUOROMETHYL)PHENYL ACETATE Basic information

Product Name:
ETHYL 4-(TRIFLUOROMETHYL)PHENYL ACETATE
Synonyms:
  • ETHYL 4-(TRIFLUOROMETHYL)PHENYL ACETATE
  • ethyl 2-(4-(trifluoromethyl)phenyl)acetate
  • REF DUPL: Ethyl 4-(trifluoromethyl)phenylacetate
  • 4-(Trifluoromethyl)benzeneacetic acid ethyl ester
  • 2-[4-(trifluoroMethyl)phenyl]butanoate
  • Benzeneacetic acid, 4-(trifluoroMethyl)-, ethyl ester
  • (4-TRIFLUOROMETHYL-PHENYL)-ACETIC ACID ETHYL ESTER
  • Ethyl 4-(trifluoromethyl)benzeneacetate
CAS:
721-63-1
MF:
C11H11F3O2
MW:
232.2
Mol File:
721-63-1.mol
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ETHYL 4-(TRIFLUOROMETHYL)PHENYL ACETATE Chemical Properties

Melting point:
34-35 °C
Boiling point:
104-105 °C(Press: 7 Torr)
Density 
1.207
storage temp. 
Sealed in dry,Room Temperature
solubility 
soluble in Methanol
form 
Solid
color 
Colorless
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36/37/39
HS Code 
2916340000
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ETHYL 4-(TRIFLUOROMETHYL)PHENYL ACETATE Usage And Synthesis

Synthesis

402-43-7

6148-64-7

721-63-1

General procedure: Under standard Schlenk operating conditions, the reaction system is first evacuated and backfilled three times with dry pure nitrogen. To a pre-dried Schlenk tube fitted with a magnetic stirring bar, palladium catalyst (see Tables 1 to 4 for specific types and amounts), ligand (see Tables 1 to 4), N,N-dimethylpyridin-4-amine (DMAP, see Tables 1 to 4), and monoethyl malonate potassium salt (see Tables 1 to 4) are added sequentially. Subsequently, the reaction tube was evacuated and backfilled with argon, and this process was repeated three times. Under argon protection, p-bromobenzotrifluoride (see Tables 1 through 4) and an appropriate amount of solvent (see Tables 1 through 4) were added via syringe. The reaction tube was sealed and stirred for 10 minutes at room temperature. Afterwards, the reaction tube is connected to a Schlenk line pre-filled with argon and placed in an oil bath preheated to 140-150°C and the reaction is stirred for 20-25 hours. After completion of the reaction, the reaction was cooled to room temperature, the reaction mixture was diluted with ether and the yield of ethyl 4-(trifluoromethyl)phenylacetate was determined by gas chromatography using 1,3-dimethoxybenzene as an internal standard.

References

[1] Tetrahedron, 2012, vol. 68, # 9, p. 2113 - 2120

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