HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1043414Generated: November 1, 2026
Water → 4-Bromo-[1,1'-biphenyl]-2-carboxylic acid
https://huagongshe.com/reaction/1043414
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Permanganate | HCID 516875 | — |
| Reactant | 4-Bromo-2-methylbiphenyl | HCID 9964845 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 4-Bromo-[1,1'-biphenyl]-2-carboxylic acid | HCID 19922469 | 89% |
Reaction Steps
4-bromo-2-methylbiphenyl (5 g, 20.23 mmol) was suspended in pyridine (23 mL) and water (35 mL). Potassium permanganate (16 g, 101 mmol) was added portion wise over a period of 20 min. The mixture was refluxed overnight. The reaction mixture was cooled and MnO2 was filtered off. Conc. HCl was added to the filtrate until the product precipitated. The product was extracted with DCM, washed with water and brine, collected, dried (MgSO4), filtered and evaporated to give 4-bromobiphenyl-2-carboxylic acid (5 g, 18.04 mmol, 89% yield) as a white solid. LCMS: rt=1.39 min.; Phenomenex-Luna C-18 (5μ) (3.0×50 mm); Solvent A=10% acetonitrile—90% water—0.1% TFA, Solvent B=90% acetonitrile—10% water—0.1% TFA; gradient 0% to 100% solvent B over 2 min. and then hold for 1 min.; 4 mL/min; inj. vol.=5 uL; wavelength=220.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08563505B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-29868b549e6142709f9143c19db7f506 |
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| Source note | uspto-grants-2013_10 |
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