Basic information Safety Supplier Related

2-(2-bromophenyl)-2-oxoacetic acid

Basic information Safety Supplier Related

2-(2-bromophenyl)-2-oxoacetic acid Basic information

Product Name:
2-(2-bromophenyl)-2-oxoacetic acid
Synonyms:
  • 2-(2-bromophenyl)-2-oxoacetic acid
  • 2-Bromobenzoylformic acid
  • Benzeneacetic acid, 2-bromo-α-oxo-
  • (2-Bromo-phenyl)-oxo-acetic acid
CAS:
26767-16-8
MF:
C8H5BrO3
MW:
229.03
Mol File:
26767-16-8.mol
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2-(2-bromophenyl)-2-oxoacetic acid Chemical Properties

Melting point:
104-107 °C
Boiling point:
330.5±34.0 °C(Predicted)
Density 
1.738±0.06 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Room Temperature
pka
1.91±0.54(Predicted)
Appearance
White to off-white Solid
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Safety Information

HazardClass 
IRRITANT
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2-(2-bromophenyl)-2-oxoacetic acid Usage And Synthesis

Synthesis

2142-69-0

26767-16-8

A solution of 1-(2-bromophenyl)ethan-1-one (10 g, 50.24 mmol, 1.00 eq.) in pyridine (80 mL) was added to a 250 mL three-necked round-bottomed flask under nitrogen protection. Selenium dioxide (22 g, 198.27 mmol, 3.95 equiv) was then added. The reaction mixture was placed in a 120°C oil bath and stirred for 18 hours. After completion of the reaction, it was cooled to room temperature and filtered to remove solids. The filtrate was concentrated under reduced pressure and the residue was dissolved in 100 mL of water. The aqueous phase was washed with ethyl acetate (2×50 mL), and then the pH of the aqueous phase was adjusted to 1-2 with 4 mol/L hydrochloric acid.The aqueous phase was extracted with ethyl acetate (3×80 mL), and the organic phases were combined and dried with anhydrous sodium sulfate. The desiccant was removed by filtration and the filtrate was concentrated under reduced pressure to give 2-(2-bromophenyl)-2-oxoacetic acid (10 g, 87% yield) as a yellow oil. Mass spectrum (ESI) m/z 230 ([M + H]+).

References

[1] Patent: WO2017/168368, 2017, A1. Location in patent: Page/Page column 17
[2] Patent: WO2014/143960, 2014, A1. Location in patent: Page/Page column 33
[3] Tetrahedron, 2007, vol. 63, # 12, p. 2695 - 2711
[4] Chemical Communications, 2013, vol. 49, # 35, p. 3640 - 3642
[5] Advanced Synthesis and Catalysis, 2013, vol. 355, # 8, p. 1517 - 1522

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