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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant2,4,6-Tribromo-3,5-difluoropyridineHCID 2778700—
Reactant2-Fluoro-5-nitrophenylboronic acid, pinacol esterHCID 3833297—
CatalystHCID 178418397HCID 178418397—
SolventTetrahydrofuranHCID 8028—
Product2,4-Dibromo-3,5-difluoro-6-(2-fluoro-5-nitrophenyl)pyridineHCID 2228527428.2%

Reaction Conditions

Temperature55 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06960598B2
Source datasetuspto-grants-2005_11
ORD IDord-fab249d3a90c4c12a7a737ca2f27166a
Source noteuspto-grants-2005_11