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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 444662Erstellt: 26. Oktober 2026

Potassium Carbonate → 9-Phenylanthracene

https://huagongshe.com/reaction/444662

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
EduktPhenylboronic AcidHCID 66827—
Edukt9-BromoanthraceneHCID 74062—
EduktTri-o-tolylphosphineHCID 80271—
Katalysatorpalladium(II) acetateHCID 167845—
Lösungsmittel1,2-DimethoxyethaneHCID 8071—
Produkt9-PhenylanthraceneHCID 1176685%

Reaktionsschritte

Into a 200 mL three-neck flask were put 5.4 g (21 mmol) of 9-bromoanthracene, 2.6 g (21 mmol) of phenylboronic acid, 60 mg (0.2 mmol) of palladium(II) acetate (abbreviation: Pd(OAc)2), 10 mL (20 mmol) of potassium carbonate aqueous solution (2.0 mol/L), 260 mg (0.8 mmol) of tris(o-tolyl)phosphine (abbreviation: P(o-tolyl)3), and 20 mL of 1,2-dimethoxyethane (abbreviation: DME), and then the mixture was stirred at 80° C. in a nitrogen atmosphere for 9 hours. After the reaction, a precipitated solid was collected by suction filtration, dissolved in toluene, and filtered through Florisil (produced by Wako Pure Chemical Industries, Ltd., Catalog No. 540-00135), celite (produced by Wako Pure Chemical Industries, Ltd., Catalog No. 531-16855), and alumina. The obtained filtrate was washed with water and saturated aqueous solution and magnesium sulfate was added so that the moisture was removed. This suspending solution was naturally filtered and the obtained filtrate was concentrated, whereby 22 g of a light-brown solid of 9-phenylanthracene, which was the object of the synthesis, was obtained in a yield of 85% (synthesis scheme (a-1)).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08475935B2
Quelldatensatzuspto-grants-2013_07
ORD IDord-bd8731d07a4b4e3abd48af477f59ad25
Quellennotizuspto-grants-2013_07