HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1061809Generated: October 26, 2026
Sodium Carbonate → 2,4-Dibromo-3,5-difluoro-6-(2-fluoro-5-nitrophenyl)pyridine
https://huagongshe.com/reaction/1061809
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2,4,6-Tribromo-3,5-difluoropyridine | HCID 2778700 | — |
| Reactant | 2-Fluoro-5-nitrophenylboronic acid, pinacol ester | HCID 3833297 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2,4-Dibromo-3,5-difluoro-6-(2-fluoro-5-nitrophenyl)pyridine | HCID 22285274 | 28.2% |
Reaction Steps
To a degassed mixture of 3,5-difluoro-2,4,6-tribromopyridine (4.26 g, 12.1 mmol), 2-(2-fluoro-5-nitrophenyl)-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane (2.80 g, 10.4 mmol), aqueous sodium carbonate (10 mL of a 2 M solution) and tetrahydrofuran (40 mL) was added tetrakis(triphenylphosphine)palladium(0) (0.67 g). The mixture was then stirred at 55° C. for 48 h under an atmosphere of nitrogen. The reaction mixture was then partitioned between water and ethyl acetate. The organic layer was separated and evaporated and the residue chromatographed on silica gel eluting with isohexane on a gradient of dichloromethane (20-40%) to afford 2,4-dibromo-3,5-difluoro-6-(2-fluoro-5-nitrophenyl)pyridine as a solid (1.21 g): δH (400 MHz, CDCl3) 7.37 (1H, t, J 9), 8.38 (1H, m), 8.55 (1H, dd, J 6 and 3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06960598B2 |
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| Source dataset | uspto-grants-2005_11 |
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| ORD ID | ord-fab249d3a90c4c12a7a737ca2f27166a |
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| Source note | uspto-grants-2005_11 |
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