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METHYL 3-FLUOROPHENYLACETATE

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METHYL 3-FLUOROPHENYLACETATE Basic information

Product Name:
METHYL 3-FLUOROPHENYLACETATE
Synonyms:
  • METHYL 3-FLUOROPHENYLACETATE
  • (3-Fluorophenyl)acetic acid methyl ester
  • 2-(3-Fluorophenyl)acetic acid methyl ester
  • 3-Fluorobenzeneacetic acid methyl ester
  • Methyl 3-fluorophenylacetate,98%
  • Methyl 2-(3-fluorophenyl)acetate
  • Methyl 2-(3-fluorophenyl)
  • Methyl 3-fluorophenylacetate, 97.5%
CAS:
64123-77-9
MF:
C9H9FO2
MW:
168.16
Mol File:
64123-77-9.mol
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METHYL 3-FLUOROPHENYLACETATE Chemical Properties

Boiling point:
204.0±15.0℃ (760 Torr)
Density 
1.148±0.06 g/cm3 (20 ºC 760 Torr)
refractive index 
1.487-1.489
Flash point:
75.3±15.3℃
storage temp. 
Sealed in dry,Room Temperature
form 
Liquid
color 
Clear colorless to slightly yellow
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22
Safety Statements 
24/25
HazardClass 
IRRITANT
HS Code 
29163990

MSDS

  • Language:English Provider:ACROS
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METHYL 3-FLUOROPHENYLACETATE Usage And Synthesis

Chemical Properties

clear colorless to slightly yellow liquid

Synthesis

67-56-1

331-25-9

64123-77-9

General steps: 1. Thionyl chloride (4.00 mL, 52.2 mmol) was slowly added to a solution of 3-fluorophenylacetic acid (24.85 g, 158 mmol) in methanol (200 mL) at 0 °C. 2. The reaction mixture was stirred at room temperature for 3 hours and then concentrated under reduced pressure to remove the solvent. 3. The concentrated residue was extracted by partitioning between 1N sodium hydroxide solution (250mL) and ethyl acetate (250mL). 4. The organic layer was separated and washed with brine (100 mL) and subsequently dried over anhydrous magnesium sulfate. 5. The desiccant was removed by filtration and the filtrate was concentrated under reduced pressure to afford the colorless oily product methyl (3-fluorophenyl)acetate (25.81 g, 97% yield). Product characterization data: 1H NMR (CDCl3) δ 3.62 (2H, s), 3.71 (3H, s), 6.92-7.09 (3H, m), 7.29 (1H, ddd, J = 7.9, 7.7, 6.0 Hz);. IR (KBr) cm-1: 3065, 3024, 3001, 1955, 2845, 1740, 1616, 1593, 1489, 1450, 1437, 1342, 1258, 1200, 1165, 1144, 1076, 1015, 955, 930.

References

[1] Bioorganic and Medicinal Chemistry, 2003, vol. 11, # 13, p. 2843 - 2866
[2] Advanced Synthesis and Catalysis, 2012, vol. 354, # 4, p. 751 - 756
[3] Bioorganic and Medicinal Chemistry, 2017, vol. 25, # 14, p. 3719 - 3735
[4] Bioorganic and Medicinal Chemistry, 2005, vol. 13, # 15, p. 4694 - 4703
[5] Tetrahedron, 2002, vol. 58, # 51, p. 10113 - 10126

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