Basic information Safety Supplier Related

2-(3-Bromophenyl)propanoic acid

Basic information Safety Supplier Related

2-(3-Bromophenyl)propanoic acid Basic information

Product Name:
2-(3-Bromophenyl)propanoic acid
Synonyms:
  • 2-M-BROMOPHENYLPROPIONIC ACID
  • 2-(3-bromophenyl)propanoicacid
  • 2-(3-BroMophenyl)Propionic Acid
  • Benzeneacetic acid, 3-bromo-a-methyl-
CAS:
53086-52-5
MF:
C9H9BrO2
MW:
229.07
Mol File:
53086-52-5.mol
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2-(3-Bromophenyl)propanoic acid Chemical Properties

Boiling point:
319.6±17.0 °C(Predicted)
Density 
1.523±0.06 g/cm3(Predicted)
storage temp. 
Storage temp. 2-8°C
solubility 
DCM, DMSO, Diethyl Ether, Methanol
form 
Solid
pka
4.17±0.10(Predicted)
color 
White
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2-(3-Bromophenyl)propanoic acid Usage And Synthesis

Uses

2-(3-Bromophenyl)propanoic Acid is an intermediate in the synthesis of Ketoprofen (K200800) related compounds.

Synthesis

1878-67-7

74-88-4

53086-52-5

Step 1. 3-Bromophenylacetic acid (1.30 g, 6 mmol) was azeotropized with 2 mL of anhydrous toluene to remove water under nitrogen protection and cooled to room temperature. To this solution was slowly added a THF solution of sodium bis(trimethylmethylsilyl)amide (14 mL, 1N, 14 mmol). After stirring the reaction for 20 minutes at room temperature, iodomethane (0.9 g, 7 mmol) was slowly added dropwise through a constant pressure dropping funnel. After 10 min of reaction, the pH of the reaction solution was adjusted to 2 with 2N HCl solution to quench the reaction. Subsequently, the reaction mixture was extracted with ethyl acetate (EtOAc) and the organic phase was dried with anhydrous sodium sulfate (Na2SO4), filtered and concentrated to dryness under reduced pressure. Purification by fast column chromatography (silica gel, eluent gradient: dichloromethane (DCM) to DCM/EtOAc=10:1 to 4:1 to 2:1) afforded the crude 2-(3-bromophenyl)propionic acid (1.13 g, 82% yield) as a colorless oil.

References

[1] Patent: WO2008/39882, 2008, A1. Location in patent: Page/Page column 171
[2] Patent: WO2008/39882, 2008, A1. Location in patent: Page/Page column 171
[3] Patent: US2008/261921, 2008, A1. Location in patent: Page/Page column 110-111
[4] Bioorganic and Medicinal Chemistry Letters, 2013, vol. 23, # 23, p. 6447 - 6454
[5] Patent: WO2016/193939, 2016, A1. Location in patent: Page/Page column 41

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