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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1775391Erstellt: 26. Oktober 2026

Ethanol → 9-Bromo-10-(naphthalen-2-yl)anthracene

https://huagongshe.com/reaction/1775391

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolHCID 702—
EduktSodium CarbonateHCID 10340—
Edukt9,10-DibromoanthraceneHCID 68226—
Edukt(Naphthalen-2-yl)boronic acidHCID 2734375—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelTolueneHCID 1140—
Produkt9-Bromo-10-(naphthalen-2-yl)anthraceneHCID 1611626361%

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

A mixture of 15 g (44.6 mmol) of 9,10-dibromoanthracene, 7.7 g (44.6 mmol) of naphthalen-2-ylboronic acid, 0.52 g (0.446 mmol) of Tetrakis(triphenylphosphine)Palladium, 33 ml of 2M Na2CO3, 60 ml of EtOH and 150 ml toluene was degassed and placed under nitrogen, and then heated at 90° C. for 24 h. After the reaction finish, the mixture was allowed to cool to room temperature. The organic layer was extracted with ethyl acetate and water, dried with anhydrous magnesium sulfate, the solvent was removed and the residue was purified by column chromatography on silica (hexane-dichloromethane) to give product 10.4 g (61%) as a yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09260363B2
Quelldatensatzuspto-grants-2016_02
ORD IDord-4c74d78cba8e4e248586496270730689
Quellennotizuspto-grants-2016_02