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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2121369Generated: November 2, 2026

Potassium Carbonate → 4-Fluoro-3-(pyridin-3-yl)aniline

https://huagongshe.com/reaction/2121369

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant3-(Diethylboryl)pyridineHCID 642851—
Reactant3-Bromo-4-fluoroanilineHCID 2779286—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
Product4-Fluoro-3-(pyridin-3-yl)anilineHCID 2228533046.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 3-bromo-4-fluorophenylamine (7.92 g, 41.7 mmol), diethyl(3-pyridyl)borane (6.74 g, 45.9 mmol), tetrakis(triphenylphosphine)palladium(0) (0.96 g, 0.83 mmol) and potassium carbonate (17.26 g, 125 mmol) in 1,2-dimethoxyethane (30 ml) and water (15 ml) was heated at 80° C. for 20 h. After cooling to ambient temperature the reaction was partitioned between ethyl acetate (500 ml) and water (500 ml). The organics were washed with brine (400 ml), dried (Na2SO4), filtered and concentrated in vacuo. Purification of the residue by flash chromatography (silica gel, 0%-20% EtOAc/CH2Cl2) gave 4-fluoro-3-(pyridin-3-yl)phenylamine (3.64 g, 46%) as a colourless oil that solidified on standing to afford a white solid: 1H NMR (360 MHz, CDCl3) δ3.65 (2H, s), 6.65-6.72 (2H, m), 6.99. (1H, dd, J 9, 9 Hz), 7.33-7.37 (1H, m), 7.84-7.86 (1H, m), 8.58 (1H, d, J 4 Hz), 8.76 (1H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06696444B2
Source datasetuspto-grants-2004_02
ORD IDord-41f5a0794cbd40b29ca88bb1ec212daf
Source noteuspto-grants-2004_02