HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 586285Generated: October 29, 2026
Water → 3-Fluoro-2-(2-fluoro-5-nitrophenyl)pyridine
https://huagongshe.com/reaction/586285
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | 2-Bromo-3-fluoropyridine | HCID 2762803 | — |
| Reactant | 2-Fluoro-5-nitrophenylboronic acid, pinacol ester | HCID 3833297 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Fluoro-2-(2-fluoro-5-nitrophenyl)pyridine | HCID 22285339 | 92.4% |
Reaction Steps
To 2-bromo-3-fluoropyridine (1.198 g, 6.807 mmol), prepared according to the procedure of Queguiner et al. (Tetrahedron, 1983, 39, 2009-21), and 2-(2-fluoro-5-nitrophenyl)-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane (2.72 g, 10.2 mmol), in dry tetrahydrofuran (20 ml) under an atmosphere of nitrogen, was added potassium fluoride (2.0 g), water (1.0 ml) and tris(dibenzylideneacetone)dipalladium(0) (0.139 g). The mixture was thoroughly degassed, then a solution of tri-tert-butylphosphine (3.05 ml of a 0.1 M solution in 1,4-dioxane) was added. The mixture was stirred at 35° C. for 18 h. The reaction was partitioned between dichloromethane and water, the organic phase separated, evaporated, and the residue chromatographed (silica gel; CH2Cl2) to afford 3-fluoro-2-(2-fluoro-5-nitrophenyl)pyridine as a white solid (1.485 g): MS (ES+) m/z 236 M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06936608B2 |
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| Source dataset | uspto-grants-2005_08 |
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| ORD ID | ord-82480af9891047318716dfc9d2b6ed64 |
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| Source note | uspto-grants-2005_08 |
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