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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1176944Erstellt: 25. Oktober 2026

Acetone → O-Terphenyl

https://huagongshe.com/reaction/1176944

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetoneHCID 180—
EduktNeopentyl glycolHCID 31344—
Edukt(4-Propylphenyl)boronic acidHCID 4100861—
EduktTrimethyl(2,3,2'-trifluoro-4'-iodobiphenyl-4-yl)silaneHCID 11304300—
Katalysatorpalladium(II) acetateHCID 167845—
LösungsmittelIsopropanolHCID 3776—
ProduktO-TerphenylHCID 676689%

Reaktionsschritte

A solution of (2 mmol) of 8, (2.2 mmol) of 4-propylphenylboronic acid, 250 mg (2.40 mmol) of neopentyl glycol, 1.53 g (4.84 mmol) of Ba(OH)2 8 H2O, 1.35 ml (0.103 mmol, 5 mol %) of a 76 mM acetone solution of Pd(OAc)2 in 20 ml of 95% i—PrOH is stirred at 80° C. for 12 hours. The solvent is subsequently removed under reduced pressure. 5 ml of 2 M HCl are added to the residue, and the mixture is extracted with dichloromethane (3×5 ml). The combined organic phases are dried over MgSO4 and filtered through SiO2. The solvent is removed under reduced pressure, and the residue is converted into 10 (yield: 89%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07842845B2
Quelldatensatzuspto-grants-2010_11
ORD IDord-de98e425693a48bca8f2833cf7957733
Quellennotizuspto-grants-2010_11