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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTris(1,1-dimethylethyl)phosphineHCID 83681—
EduktPotassium FluorideHCID 522689—
Edukt2-Methoxyphenylboronic acidHCID 2733958—
EduktTris(2-bromo-6-pyridyl)phosphine oxideHCID 21708779—
Katalysatorpalladium(II) acetateHCID 167845—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
ProduktTris(6-(2-methoxyphenyl)-2-pyridyl)phosphine oxideHCID 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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07728137B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-e8606940710b406b8029a0d140bc9a4d
Quellennotizuspto-grants-2010_06