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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 537591Erstellt: 23. Oktober 2026

Potassium Carbonate → 9-Phenylanthracene

https://huagongshe.com/de/reaction/537591

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%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

5.4 g (21.1 mmol) of 9-bromoanthracene, 2.6 g (21.1 mmol) of phenylboronic acid, 60 mg (0.21 mmol) of palladium(II) acetate (abbreviation: Pd(OAc)2), 10 mL (20 mmol) of a potassium carbonate aqueous solution (2 mol/L), 263 mg (0.84 mmol) of tris(ortho-tolyl)phosphine (abbreviation: P(o-tolyl)3), and 20 mL of 1,2-dimethoxyethane (abbreviation: DME) were put in a 200 mL three neck flask, and then stirred for nine hours at 80° C. in nitrogen stream. After reaction, a precipitated solid was collected by suction filtration. Subsequently, the solid was dissolved in toluene and then filtered through florisil, celite, and alumina. After a filtrate was washed with water and saturated saline, it was dried with magnesium sulfate. After the mixture was subjected to natural filtration, when the filtrate was concentrated, 21.5 g of 9-phenylanthracene which was a target substance was obtained as a light brown solid at a yield of 85% (Synthesis scheme (b-1)).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08860019B2
Quelldatensatzuspto-grants-2014_10
ORD IDord-4e389874e59f47cf8a297b6f7d703899
Quellennotizuspto-grants-2014_10