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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 219830Generated: October 29, 2026

Potassium Fluoride → Methyl 2'-methyl-2-(methylsulfonyl)biphenyl-4-carboxylate

https://huagongshe.com/reaction/219830

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium FluorideHCID 522689—
Reactant2-Methylphenyl boronic acidHCID 2733267—
ReactantMethyl 4-chloro-3-(methylsulfonyl)benzoateHCID 10490815—
Reactant2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
Catalystpalladium(II) acetateHCID 167845—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductMethyl 2'-methyl-2-(methylsulfonyl)biphenyl-4-carboxylateHCID 6752838288.7%

Reaction Steps

In a schlenk flushed with Argon were added methyl 4-chloro-3-(methylsulfonyl)benzoate (124.34 mg; 0.50 mmol; 1 eq.), o-tolylboronic acid (84.97 mg; 0.62 mmol; 1.25 eq.), palladium(II) acetate (22.45 mg; 0.10 mmol; 0.20 eq.), 2-dicyclohexylphosphino-2′,6′-dimethoxy-1,1′-biphenyl (82.11 mg; 0.20 mmol; 0.40 eq.), potassium fluoride (87.14 mg; 1.50 mmol; 3 eq.), toluene (2.49 mL), MeOH (2.49 mL) and water (5.40 μl). The reaction was degassed with Ar and heated under reflux for 2 hours. Then, it was cooled down to RT. The solvents were evaporated and the crude mixture was dissolved in EtOAc, washed with water and brine and dried over MgSO4. The resulting crude product was purified by flash chromatography (c-hex/EtOAc 9:1 to 5:5), affording the title compound as a light yellow oil (135 mg; 88%). 1H NMR (DMSO-d6, 300 MHz) δ 8.89 (d, J=1.77 Hz, 1H), 8.32 (dd, J=1.77, 7.90 Hz, 1H), 7.43-7.19 (m, 5H), 4 (s, 3H), 2.76 (s, 3H), 2.09 (s, 3H). LC/MS (Method B): 305.1 (M+H)+. HPLC (max plot) 99.2%; Rt 4.51 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202865B2
Source datasetuspto-grants-2012_06
ORD IDord-1f2d047105c649f6b7e09107e97eb42e
Source noteuspto-grants-2012_06