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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 537592Erstellt: 24. Oktober 2026

9-Phenylanthracene → 9-Bromo-10-phenyl-anthracene

https://huagongshe.com/de/reaction/537592

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt9-PhenylanthraceneHCID 11766—
EduktBromineHCID 24408—
EduktSodium ThiosulfateHCID 24477—
LösungsmittelCarbon TetrachlorideHCID 5943—
Produkt9-Bromo-10-phenyl-anthraceneHCID 415583689%

Reaktionsschritte

6.0 g (23.7 mmol) of 9-phenylanthracene was dissolved in 80 mL of carbon tetrachloride, and then, in the reaction solution thereof, a solution in which 3.80 g (21.1 mmol) of bromine was dissolved in 10 mL of carbon tetrachloride was dropped by a dropping funnel. After dropping, it was stirred for one hour at room temperature. After reaction, a sodium thiosulfate aqueous solution was added thereto and stirred. An organic layer was washed with a sodium hydroxide aqueous solution and saturated saline, and then dried with magnesium sulfate. After the mixture was subjected to natural filtration, the filtrate was concentrated and dissolved in toluene, and then filtration was carried out using florisil, celite, and alumina. When the filtrate was concentrated and then recrystallized with a mixed solution of dichloromethane and hexane, 7.0 g of 9-bromo-10-phenylanthracene that was a target substance was obtained as a light yellow solid at a yield of 89% (Synthesis scheme (b-2)).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08860019B2
Quelldatensatzuspto-grants-2014_10
ORD IDord-7b6fe09197b24aeeb27eeba13a29b3e4
Quellennotizuspto-grants-2014_10