HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 42033Erstellt: 23. Oktober 2026
1,3-Difluorobenzene → 6-(2,6-Difluorophenyl)pyridin-3-amine
https://huagongshe.com/de/reaction/42033
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1,3-Difluorobenzene | HCID 9741 | — |
| Edukt | 6-Bromopyridin-3-amine | HCID 642811 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Katalysator | Zincchloride | HCID 3007855 | — |
| Katalysator | HCID 178418397 | HCID 178418397 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 6-(2,6-Difluorophenyl)pyridin-3-amine | HCID 58415875 | 30,2% |
Reaktionsschritte
In a three neck round bottle flask, to a mixture of 1,3-difluorobenzene (23.24 mmol, 2.29 ml) in THF (30 ml) at −78° C. under argon atmosphere, a solution of n-BuLi (10.2 ml) in THF (2.5M) was added. The mixture was stirred at −78° C. for 30 minutes and then it was heated to −50° C. A solution of ZnCl2 (51 ml) in THF (0.5M) was added drop wise and the mixture was stirred at this temperature for 20 minutes. A solution of 6-bromopyridin-3-amine (11.56 mmol, 2.0 g) in THF (20 ml) and Pd(PPh3)4 (1.16 mmol, 1.3 g) were added respectively and the crude mixture was heated at 40° C. overnight. The solvent was evaporated and the crude mixture was purified by reverse phase chromatography eluting with a water-MeOH/AcN system affording 0.72 g (yield 30%) of the expected product.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08536165B2 |
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| Quelldatensatz | uspto-grants-2013_09 |
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| ORD ID | ord-887e871e69e540029f5e78fea7682c0c |
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| Quellennotiz | uspto-grants-2013_09 |
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