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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2266323Generated: October 26, 2026

Potassium Phosphate, Tribasic → 5-(2-Chlorophenyl)-4-(4-chlorophenyl)-2-fluoropyridine

https://huagongshe.com/reaction/2266323

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant2-Chlorophenylboronic acidHCID 2734322—
Reactant2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
Reactant5-Chloro-4-(4-chlorophenyl)-2-fluoropyridineHCID 57799455—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Product5-(2-Chlorophenyl)-4-(4-chlorophenyl)-2-fluoropyridineHCID 5779941235.4%

Reaction Conditions

Temperature95 °C

Reaction Steps

To a flame-dried tube was placed 5-chloro-4-(4-chlorophenyl)-2-fluoropyridine (0.71 g, 2.93 mmol), 2-chlorophenylboronic acid (0.55 g, 3.52 mmol), K3PO4 (1.24 g, 5.86 mmol), Pd2(dba)3 (0.134 g, 0.147 mmol), and S-Phos (0.12 g, 0.29 mmol). The reaction vessel was then purged with argon three times before degassed toluene (15 mL) was added in, and sealed. The reaction mixture was stirred at 95° C. for 16 h. Analysis by HPLC/MS indicated the reaction was complete. After cooling to room temperature, the reaction mixture was partitioned between EtOAc and water. The aqueous layer was extracted with EtOAc (30 mL×3). The combined organic was washed with saturated aqueous NaCl, dried over Na2SO4, filtered and concentrated under reduced pressure. The crude product was purified using a silica gel cartridge (80 g) eluting with a gradient of EtOAc (0-10%) in hexanes to afford 0.33 g (35%) of the title compound as a white foam. HPLC/MS: retention time=4.03 min, [M+H]+=318.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07858639B2
Source datasetuspto-grants-2010_12
ORD IDord-1c5530d1021846e8815c4313f6824610
Source noteuspto-grants-2010_12