2-(4-bromo-2-chlorophenyl)acetic acid

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2-(4-bromo-2-chlorophenyl)acetic acid manufacturers

2-(4-bromo-2-chlorophenyl)acetic acid Basic information
Product Name:2-(4-bromo-2-chlorophenyl)acetic acid
Synonyms:2-(4-bromo-2-chlorophenyl)acetic acid;Benzeneacetic acid, 4-broMo-2-chloro-;4-Bromo-2-chlorobenzeneacetic acid
CAS:916516-89-7
MF:C8H6BrClO2
MW:249.49
EINECS:
Product Categories:
Mol File:916516-89-7.mol
2-(4-bromo-2-chlorophenyl)acetic acid Structure
2-(4-bromo-2-chlorophenyl)acetic acid Chemical Properties
Boiling point 353.2±27.0 °C(Predicted)
density 1.720±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
pka3.92±0.10(Predicted)
AppearanceWhite to off-white Solid
Safety Information
HS Code 2918999090
MSDS Information
2-(4-bromo-2-chlorophenyl)acetic acid Usage And Synthesis
Synthesis
(4-BROMO-2-CHLOROPHENYL)ACETONOTRILE

67197-54-0

2-(4-bromo-2-chlorophenyl)acetic acid

916516-89-7

In a round-bottomed flask, 2-chloro-4-bromophenylacetonitrile (19.0 g, 82.4 mmol, 1.0 eq.) was dissolved in water (196 mL), followed by the addition of potassium hydroxide (KOH, 23.1 g, 412 mmol, 5.0 eq.). The reaction mixture was heated to reflux and stirred for 12-18 hours. After completion of the reaction, it was cooled to room temperature and washed with ethyl acetate (EtOAc) to remove organic impurities. The aqueous phase was acidified with 2N hydrochloric acid to pH < 2 and subsequently extracted with ethyl acetate (150 mL x 3). The organic phases were combined, washed with saturated sodium chloride solution (brine), dried over anhydrous magnesium sulfate (MgSO4), filtered and concentrated under reduced pressure to afford 2-(4-bromo-2-chlorophenyl)acetic acid (S3) as brown crystals (19.1 g, 93% yield). The product characterization data were in agreement with literature reports. [20]

References[1] Tetrahedron Letters, 2016, vol. 57, # 3, p. 449 - 451
[2] Patent: WO2013/43232, 2013, A2. Location in patent: Paragraph 00502
[3] Patent: EP2017257, 2009, A1. Location in patent: Page/Page column 21-22
[4] Patent: JP2015/231988, 2015, A. Location in patent: Paragraph 0361; 0362
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