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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 68528Erstellt: 23. Oktober 2026

Hydrochloric Acid → 2,10-Di(2-naphthyl)anthracene

https://huagongshe.com/de/reaction/68528

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
Edukt2-BromonaphthaleneHCID 11372—
Edukt2-(2-Naphthyl)-10-anthroneHCID 58194450—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelHexaneHCID 8058—
Produkt2,10-Di(2-naphthyl)anthraceneHCID 5819427632%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

Under an argon atmosphere, a solution of 4.81 g of 2-bromonaphthalene in 30 mL of THF was cooled to −78° C. Subsequently, 25 mL of a 1.6-M solution of n-butyllithium in hexane were dropped to the solution, and then the mixture was stirred at −78° C. for 1 hour. A solution of 6.76 g of 2-(2-naphthyl)-10-anthrone in 20 mL of THF was added to the mixture, and then the resultant reaction solution was stirred for 5 hours at 50° C. under heat. After the reaction solution had been cooled to room temperature, 100 mL of 10% hydrochloric acid were added to the solution. After the water layer had been removed, the organic layer was washed with water and a saturated salt solution. Then, the organic layer was dried with magnesium sulfate. The solvent was removed by distillation under reduced pressure, and then the residue was purified by silica gel column chromatography. Thus, 2.90 g of 2,10-di(2-naphthyl)anthracene were obtained (in 32% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08822041B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-9b4acf6cbeac4810b14a951005e380ec
Quellennotizuspto-grants-2014_09