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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1928974Erstellt: 25. Oktober 2026

Bromine → 9-Bromo-10-(4-trifluoromethylphenyl)anthracene

https://huagongshe.com/reaction/1928974

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBromineHCID 24408—
EduktSodium ThiosulfateHCID 24477—
Edukt9-[4-(Trifluoromethyl)phenyl]anthraceneHCID 264463—
LösungsmittelCarbon TetrachlorideHCID 5943—
Produkt9-Bromo-10-(4-trifluoromethylphenyl)anthraceneHCID 58163294—

Reaktionsschritte

5.7 g (18 mmol) of 9-(4-trifluoromethylphenyl)anthracene and 90 mL of carbon tetrachloride were put into a 500-mL three-neck flask and stirred. A solution in which 3.2 g (20 mmol) of bromine was dissolved in 10 mL of carbon tetrachloride was dropped into the above solution through a dropping funnel. After that, the solution was stirred at the room temperature for 1 hour, and a sodium thiosulfate aqueous solution was added to the reaction solution to complete the reaction. A water layer of the reaction mixture was extracted by chloroform, and the extracted solution and an organic layer were together washed with a saturated sodium hydrogen carbonate solution and saturated saline. The organic layer was dried with magnesium sulfate, and the mixture was filtrated naturally to remove the magnesium sulfate. Then, the filtrate was condensed to obtain a solid. The obtained solid was recrystallized with ethanol, whereby 5.9 g of a yellow powdery solid, which was a target matter, was obtained with the yield of 84%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08183793B2
Quelldatensatzuspto-grants-2012_05
ORD IDord-1a30691f77504676bb91748707fda123
Quellennotizuspto-grants-2012_05