HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 42006Erstellt: 26. Oktober 2026
3,5-Difluoroanisole → 5-Bromo-2-(2,6-difluoro-4-methoxyphenyl)pyrimidine
https://huagongshe.com/reaction/42006
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 3,5-Difluoroanisole | HCID 2724518 | — |
| Edukt | 5-Bromo-2-iodopyrimidine | HCID 7006651 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Katalysator | Zincchloride | HCID 3007855 | — |
| Katalysator | HCID 178418397 | HCID 178418397 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 5-Bromo-2-(2,6-difluoro-4-methoxyphenyl)pyrimidine | HCID 67394249 | — |
Reaktionsschritte
In a three neck round bottle flask, to a mixture of 1,3-difluoro-5-methoxybenzene (8.39 mmol, 0.98 ml) in THF (40 ml) at −78° C. under argon atmosphere, a solution of n-BuLi (9.13 mmol, 3.65 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 (9.13 mmol, 18.3 ml) in THF (0.5M) was added dropwise and the mixture was stirred at this temperature for 20 minutes. A solution of 5-bromo-2-iodopyrimidine (7.02 mmol, 2.0 g) in THF (5 ml) and Pd(PPh3)4 (0.70 mmol, 0.81 g) were added respectively and the crude mixture was heated at 40° C. overnight. The solvent was evaporated and the crude mixture was purified over SiO2 eluting with mixtures of hexane/ethyl acetate affording 0.89 g (39% of yield) 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-4d16c8f35f0c41efab5adb9498d52603 |
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| Quellennotiz | uspto-grants-2013_09 |
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