HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 13635Erstellt: 24. Oktober 2026
Tris(1,1-dimethylethyl)phosphine → Tris(6-(2-methoxyphenyl)-2-pyridyl)phosphine oxide
https://huagongshe.com/de/reaction/13635
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Tris(1,1-dimethylethyl)phosphine | HCID 83681 | — |
| Edukt | Potassium Fluoride | HCID 522689 | — |
| Edukt | 2-Methoxyphenylboronic acid | HCID 2733958 | — |
| Edukt | Tris(2-bromo-6-pyridyl)phosphine oxide | HCID 21708779 | — |
| Katalysator | palladium(II) acetate | HCID 167845 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | Tris(6-(2-methoxyphenyl)-2-pyridyl)phosphine oxide | HCID 86608172 | — |
Reaktionsschritte
An efficiently stirred suspension of 38.8 g (75.0 mmol) of tris(2-bromo-6-pyridyl)phosphine oxide, 51.3 g (337.5 mmol) of 2-methoxybenzeneboronic acid and 43.1 g (742.5 mmol) of potassium fluoride in 750 ml of anhydrous THF was admixed with 593 mg (2.93 mmol) of tri-tert-butylphosphine and then with 505 mg (2.25 mmol) of palladium(II) acetate, and subsequently heated under reflux for 16 h. After cooling, the reaction mixture was admixed with 1500 ml of ethyl acetate and 1000 ml of water. The organic phase was removed, washed twice with 500 ml of water and once with 500 ml of sat. sodium chloride solution, and subsequently dried over magnesium sulfate. After the organic phase had been concentrated under reduced pressure (end pressure 1 mbar, temperature 90° C.), 44.3 g (98.5%) of a pale yellow highly viscous oil remained, which was reacted further without purification.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07728137B2 |
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| Quelldatensatz | uspto-grants-2010_06 |
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| ORD ID | ord-e8606940710b406b8029a0d140bc9a4d |
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| Quellennotiz | uspto-grants-2010_06 |
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