Basic information Safety Supplier Related

2-(4-fluorophenyl)propionic acid

Basic information Safety Supplier Related

2-(4-fluorophenyl)propionic acid Basic information

Product Name:
2-(4-fluorophenyl)propionic acid
Synonyms:
  • 2-(4-fluorophenyl)propionic acid
  • 4-Fluoro-alpha-methylphenylaceticacid
  • 2-(4-Fluorophenyl)propanoic acid
  • 4-Fluoro-α-methylbenzeneacetic acid
  • 4-Fluoro-alpha-methylphenylacetic acid,98%
  • (+/-)-2-(4-flurophenyl)propanoic acid
  • Benzeneacetic acid, 4-fluoro-α-methyl-
  • Benzeneacetic acid,4-fluoro-a-methyl-
CAS:
75908-73-5
MF:
C9H9FO2
MW:
168.16
EINECS:
278-340-6
Mol File:
75908-73-5.mol
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2-(4-fluorophenyl)propionic acid Chemical Properties

Boiling point:
258.8±15.0 °C(Predicted)
Density 
1?+-.0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
form 
solid
pka
4.31±0.10(Predicted)
color 
Off-white
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Safety Information

RIDADR 
2811
HazardClass 
6.1
PackingGroup 
HS Code 
2918199890
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2-(4-fluorophenyl)propionic acid Usage And Synthesis

Synthesis

50415-71-9

75908-73-5

The general procedure for the synthesis of 2-(4-fluorophenyl)propionic acid from the compound (CAS: 50415-71-9) was as follows: under stirring conditions, racemic methyl 2-(4-thieno-phenyl)propionate (18.9 g) was dissolved in ethanol (200 mL) and an aqueous solution of potassium hydroxide (35 g) (200 mL) was slowly added. The reaction mixture was stirred continuously at 0 °C for 4 hours. Upon completion of the reaction, the pH was adjusted to 5 with 4.0 M hydrochloric acid, followed by extraction of the reaction mixture with ethyl acetate. The organic phase was separated and the solvent was removed by distillation under reduced pressure to give 15.64 g of 2-(4-fluorophenyl)propionic acid as a crude product. The crude product could be used directly in the subsequent reaction without further purification. The structure of the product was confirmed by 1H-NMR (300 MHz, DMSO-d6): δ [ppm] = 1.31 (d, 3H), 3.66 (q, 1H), 7.05-7.15 (m, 2H), 7.24-7.33 (m, 2H), 12.30 (s, 1H).

References

[1] Organic letters, 2002, vol. 4, # 3, p. 371 - 373
[2] Journal of Organic Chemistry, 2003, vol. 68, # 19, p. 7234 - 7242
[3] Patent: WO2010/31183, 2010, A1. Location in patent: Page/Page column 18
[4] Patent: WO2013/87579, 2013, A1. Location in patent: Page/Page column 134; 135
[5] Patent: WO2014/9219, 2014, A1. Location in patent: Page/Page column 107; 108

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