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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 2-Chlorophenylboronic acid | HCID 2734322 | — |
| Reactant | 2-Dicyclohexylphosphino-2',6'-dimethoxybiphenyl | HCID 11269872 | — |
| Reactant | 5-Chloro-4-(4-chlorophenyl)-2-fluoropyridine | HCID 57799455 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Product | 5-(2-Chlorophenyl)-4-(4-chlorophenyl)-2-fluoropyridine | HCID 57799412 | 35.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07858639B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-1c5530d1021846e8815c4313f6824610 |
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| Source note | uspto-grants-2010_12 |
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