2-(4-Bromophenyl)-2-oxoacetic acid

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2-(4-Bromophenyl)-2-oxoacetic acid Basic information
Product Name:2-(4-Bromophenyl)-2-oxoacetic acid
Synonyms:2-(4-Bromophenyl)-2-oxoacetic acid;Benzeneacetic acid, 4-bromo-α-oxo-;4-Bromophenylglyoxylic acid
CAS:7099-87-8
MF:C8H5BrO3
MW:229.03
EINECS:
Product Categories:
Mol File:7099-87-8.mol
2-(4-Bromophenyl)-2-oxoacetic acid Structure
2-(4-Bromophenyl)-2-oxoacetic acid Chemical Properties
Melting point 89 °C
Boiling point 152-155 °C(Press: 3 Torr)
density 1.738±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
pka2.03±0.54(Predicted)
AppearanceWhite to off-white Solid
Safety Information
MSDS Information
2-(4-Bromophenyl)-2-oxoacetic acid Usage And Synthesis
Synthesis
1-(4-BROMO-PHENYL)-2-[2-(4-BROMO-PHENYL)-2-OXO-ETHYLSULFANYL]-ETHANONE

58881-56-4

2-(4-Bromophenyl)-2-oxoacetic acid

7099-87-8

The general procedure for the synthesis of 2-(4-bromophenyl)-2-oxoacetic acid from the compound (CAS: 58881-56-4) was as follows: selenium dioxide (1.5 mmol) was dissolved in 1,4-dioxane (10.0 mL) and the solution was transferred to a 50 mL round bottom flask. Subsequently, dibenzoyl sulfide derivative 1 (0.5 mmol) was added to the solution and the reaction mixture was heated to reflux for 2 hours. The reaction process was monitored by thin layer chromatography (TLC). Upon completion of the reaction, the mixture was filtered to remove insoluble impurities and the solvent was subsequently evaporated under reduced pressure. The crude product was purified by column chromatography using a solvent mixture of petroleum ether and ethyl acetate (90:10, v/v) as eluent to give the final target product 2-(4-bromophenyl)-2-oxoacetic acid.

References[1] Journal of Sulfur Chemistry, 2014, vol. 35, # 1, p. 24 - 30
2-(4-Bromophenyl)-2-oxoacetic acid Preparation Products And Raw materials
Raw materials1-(4-Bromo-phenyl)-2-[2-(4-bromo-phenyl)-2-oxo-ethylsulfanyl]-ethanone-->1,4-Dioxane-->Selenium dioxide
Preparation ProductsEthyl 4-bromobenzoate-->Methanone, (4-bromophenyl)-1H-indol-3-yl-
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