HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1918470Generated: November 3, 2026
Potassium Carbonate → 2'Methoxy-5-(trifluoromethyl)-2,4'-bipyridine
https://huagongshe.com/reaction/1918470
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Bromo-5-(trifluoromethyl)pyridine | HCID 2736434 | — |
| Reactant | 2-Methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine | HCID 44754862 | — |
| Catalyst | Palladium Chloride | HCID 24290 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 2'Methoxy-5-(trifluoromethyl)-2,4'-bipyridine | HCID 57514760 | 73.2% |
Reaction Steps
2-Bromo-5-trifluoromethylpyridine (410 mg, 2.13 mmol), 2-methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine (500 mg, 1.81 mmol), K2CO3 (749 mg, 5.43 mmol) ανδ PdCl2 (dppf) (140 mg, 0.18 mmol) were stirred in DMSO (10 mL). The reaction mixture was degassed, then back-filled with N2. The reaction mixture was stirred at 80° C. in a pre-heated oil bath for 2 hours. After cooling, the reaction was quenched with water and extracted with CH2Cl2. The organic layer was washed with H2O and 5% LiCl, dried with Na2SO4, filtered and concentrated. Flash chromatography (silica gel, hexanes/EtOAc, 100:0 to 50:50) afforded the title compound title compound (337 mg, 62%) as a white solid: 1H NMR (300 MHz, CDCl3) δ 8.96 (s, 1H), 8.31 (d, J=5.4 Hz, 1H), 8.04 (dd, J=8.3, 2.1 Hz, 1H), 7.87 (d, J=8.3 Hz, 1H), 7.51 (dd, J=5.4, 1.4 Hz, 1H), 7.36 (s, 1H), 3.52 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08618299B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-1fea5f7bbcc8420c96e08ac383ba1bfc |
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| Source note | uspto-grants-2013_12 |
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