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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium FluorideHCID 522689—
Reactant2-Bromo-3-fluoropyridineHCID 2762803—
Reactant2-Fluoro-5-nitrophenylboronic acid, pinacol esterHCID 3833297—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTetrahydrofuranHCID 8028—
Product3-Fluoro-2-(2-fluoro-5-nitrophenyl)pyridineHCID 2228533992.4%

Reaction Conditions

Temperature35 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06936608B2
Source datasetuspto-grants-2005_08
ORD IDord-82480af9891047318716dfc9d2b6ed64
Source noteuspto-grants-2005_08