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METHYL 3-(TRIFLUOROMETHYL)PHENYLACETATE

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METHYL 3-(TRIFLUOROMETHYL)PHENYLACETATE Basic information

Product Name:
METHYL 3-(TRIFLUOROMETHYL)PHENYLACETATE
Synonyms:
  • (3-TRIFLUOROMETHYLPHENYL) ACETIC ACID METHYL ESTER
  • METHYL 3-(TRIFLUOROMETHYL)PHENYLACETATE
  • AURORA KA-6005
  • Methyl 3-(trifluoromethyl)phenylacetate 97%
  • Methyl 3-(trifluoromethyl)phenylacetate,97%
  • Methyl 2-[3-(trifluoromethyl)phenyl]acetate
  • Methyle3-(trifluoromethyl)phenylacetate
  • Methyl 2-(3-(
CAS:
62451-84-7
MF:
C10H9F3O2
MW:
218.17
Mol File:
62451-84-7.mol
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METHYL 3-(TRIFLUOROMETHYL)PHENYLACETATE Chemical Properties

Boiling point:
211℃
Density 
1.24
refractive index 
1.45-1.452
storage temp. 
Sealed in dry,Room Temperature
form 
Liquid
color 
Clear colorless
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
37/39-26
HazardClass 
IRRITANT
HS Code 
29163900

MSDS

  • Language:English Provider:ACROS
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METHYL 3-(TRIFLUOROMETHYL)PHENYLACETATE Usage And Synthesis

Chemical Properties

clear colorless liquid

Synthesis

67-56-1

351-35-9

62451-84-7

Concentrated sulfuric acid (50 mL) was added slowly to a solution of methanol (1200 mL) of m-trifluoromethylphenylacetic acid (1.0 mol). The reaction mixture was heated to reflux and the reaction was stirred overnight. Upon completion of the reaction, the reaction solution was concentrated to dryness under reduced pressure. Water (600 mL) was added to the residue and extracted with ethyl acetate (3 x 400 mL). The organic layers were combined and washed with water until neutral. The organic layer was dried with anhydrous sodium sulfate, filtered and concentrated. The crude product was purified by column chromatography (eluent: ethyl acetate/petroleum ether=1:20) to afford methyl 3-trifluoromethylphenylacetate (108 g, 100% yield) as a yellow oil.

References

[1] Bioorganic and Medicinal Chemistry, 2003, vol. 11, # 13, p. 2843 - 2866
[2] Patent: US2005/234046, 2005, A1. Location in patent: Page/Page column 97
[3] Helvetica Chimica Acta, 1971, vol. 54, p. 868 - 897
[4] Tetrahedron Letters, 2018, vol. 59, # 22, p. 2161 - 2166
[5] Patent: US2479295, 1946,

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