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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 535238Erstellt: 24. Oktober 2026

Toluene → 3-(Anthracen-9-yl)pyridine

https://huagongshe.com/de/reaction/535238

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTolueneHCID 1140—
EduktSodium CarbonateHCID 10340—
Edukt3-BromopyridineHCID 12286—
Edukt9-Anthraceneboronic AcidHCID 15510213—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
Produkt3-(Anthracen-9-yl)pyridineHCID 264388—

Reaktionsschritte

In a 200 mL three-neck flask, 5.2 g (23 mmol) of 9-anthrylboronic acid, 4.0 g (25 mmol) of 3-bromopyridine, 5.2 g (50 mmol) of sodium carbonate, 50 mL of toluene, 25 μL of ethanol, and 25 mL of water were placed. The mixture was degassed by being stirred under reduced pressure, and the air in the flask was replaced with nitrogen. To the mixture, 0.28 g (0.25 mmol) of tetrakis(triphenylphosphine)palladium(0) was added, and the mixture was stirred under nitrogen stream at 80° C. for 7 hours. After a certain period, water was added to the mixture, and an aqueous layer was extracted with toluene. The obtained extracted solution and the organic layer were combined, washed with saturated saline, and dried with magnesium sulfate. The obtained mixture was gravity filtered, and the filtrate was condensed to give an oily substance. The oily substance was recrystallized with toluene/hexane, so that 2.8 g of target yellow powder was obtained in a yield of 46%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08859108B2
Quelldatensatzuspto-grants-2014_10
ORD IDord-dd4688f4826642aca41ac290afdcfd0a
Quellennotizuspto-grants-2014_10