HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 586229Generated: October 25, 2026
Potassium Carbonate → 4-Fluoro-3-(pyridin-3-yl)aniline
https://huagongshe.com/reaction/586229
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-(Diethylboryl)pyridine | HCID 642851 | — |
| Reactant | 3-Bromo-4-fluoroaniline | HCID 2779286 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 4-Fluoro-3-(pyridin-3-yl)aniline | HCID 22285330 | 46.4% |
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) δ 3.65 (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
| 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-cb458eb9644c43d6a23e54175edf0827 |
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| Source note | uspto-grants-2005_08 |
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