HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1360692Generated: November 1, 2026
Ethanol → 2-(4-Bromo-2,6-difluorobenzyl)-6-(2,4-difluorophenyl)pyridine
https://huagongshe.com/reaction/1360692
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2,4-Difluorophenylboronic acid | HCID 2734334 | — |
| Reactant | 2-Bromo-6-(4-bromo-2,6-difluorobenzyl)pyridine | HCID 57700371 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-(4-Bromo-2,6-difluorobenzyl)-6-(2,4-difluorophenyl)pyridine | HCID 57700366 | 88.9% |
Reaction Steps
To a solution of 2-bromo-6-(4-bromo-2,6-difluorobenzyl)pyridine (from Step C above, 7.41 g, 20.53 mmol) in toluene (200 mL) was added (2,4-difluorophenyl)boronic acid (3.89 g, 24.63 mmol), tetrakis(triphenylphosphine)palladium (2.37 g, 2.05 mmol), ethanol (20 mL) and 2M Na2CO3 (20 mL). The reaction was heated to 90° C. until complete. The mixture was cooled to room temperature and concentrated. The crude residue was diluted with EtOAc/water (1:1) and washed with 1N HCl (2×), brine (3×), dried over MgSO4, and concentrated in vacuo. The crude material was purified via silica gel chromatography (hexanes/ethyl acetate) to give the title compound (7.23 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07879875B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-482ddb4600564ed49432b5d08b7aae13 |
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| Source note | uspto-grants-2011_02 |
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