HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1457740Generated: October 30, 2026
1-Bromo-4-fluorobenzene → 2-Fluoro-6-(4-fluorophenyl)pyridine
https://huagongshe.com/reaction/1457740
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Bromo-4-fluorobenzene | HCID 9993 | — |
| Reactant | 2,6-Difluoropyridine | HCID 73934 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-Fluoro-6-(4-fluorophenyl)pyridine | HCID 15431072 | 41.4% |
Reaction Steps
Butyl lithium (105.0 mL, 0.26 mol, 2.5M solution in hexane) is added to a solution of 1-bromo-4-fluoro benzene (34.3 mL, 0.31 mol) in anhydrous diethyl ether (200 mL) at -20° C. The mixture is stirred for 60 min and then chilled to -40° C. 2,6-Difluoropyridine (22.7 mL, 0.25 mol) is added and the reaction mixture is allowed to warm to ambient temperature. Subsequently, the mixture is washed with saturated aqueous ammonium chloride (300 mL). The layers are separated and the aqueous layer is washed with diethyl ether 3 times (100 mL each). After drying of the combined organic layers with anhydrous magnesium sulphate, the solvent is removed in vacuo. The crude product is purified by flash column chromatography (silica gel, hexane/AcOEt 8/2) yielding colorless crystals of 2-fluoro-6-(4'-fluorophenyl)-pyridine (19.8 g, 41.0% of th.) with mp 34° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05849758 |
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| Source dataset | uspto-grants-1998_12 |
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| ORD ID | ord-68ceeba76a6447ef8a6ff0b283959347 |
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| Source note | uspto-grants-1998_12 |
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