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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 431413Erstellt: 23. Oktober 2026

Hydrochloric Acid → HCID 18761057, Verbindung

https://huagongshe.com/de/reaction/431413

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktAnthroneHCID 7018—
EduktMagnesiumHCID 5462224—
Edukt4-Bromo-1,1'-binaphthaleneHCID 6425837—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 18761057HCID 18761057—

Reaktionsschritte

4-bromo-1,1′-binaphthyl and magnesium were refluxed in diethylether for one hour, which was then added to a solution of anthrone in tetrahydrofuran. The resulting mixture was heated for two hours, which was then poured into diluted hydrochloric acid. After being extracted by diethylether, organic layer was separated and dried over magnesium sulfate. It was purified according to conventional method, whereby 1-(9-anthryl)-4-(1-naphthyl)-naphthalene was obtained. This was dissolved in chloroform to which was added two equivalent amounts of N-bromosuccinimide, and they were stirred at room temperature for one day. The product was purified according to conventional method and 1-(10-bromo-9-anthryl)-4-(4-bromo-1-naphthyl)-naphthalene was obtained. With this pdoruct, diphenylamine was reacted in nitrobenzene at 180° C. for 40 hours together with potasium carbonate and copper powder. After nitrobenzene was removed by vacuum distillation, the reaction mixture was purified according to conventional method, whereby the target compound (18) was obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06660408B1
Quelldatensatzuspto-grants-2003_12
ORD IDord-1701c653018c44508d919f3fef87ec1e
Quellennotizuspto-grants-2003_12