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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1890629Erstellt: 25. Oktober 2026

Azobisisobutyronitrile → 3-(Bromomethyl)benzophenone

https://huagongshe.com/reaction/1890629

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAzobisisobutyronitrileHCID 6547—
EduktN-bromobutanimideHCID 67184—
Edukt3-MethylbenzophenoneHCID 69511—
LösungsmittelCarbon TetrachlorideHCID 5943—
Produkt3-(Bromomethyl)benzophenoneHCID 8958677%

Reaktionsbedingungen

Temperatur75 °C

Reaktionsschritte

Commercially available 3-methylbenzophenone (4.00 g, 20.4 mmol) was dissolved in carbon tetrachloride (100 mL), and N-bromosuccinimide (4.71 g, 26.5 mmol) and 2,2′-azobisisobutyronitrile (1.00 g, 6.09 mmol) was added to the solution, followed by stirring at 75° C. for 6.5 hours. After the reaction mixture was cooled, the precipitates were filterd out. The filtrate was combined and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:20) to obtain 3-bromomethylbenzophenone (4.31 g, yield 77%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08507484B2
Quelldatensatzuspto-grants-2013_08
ORD IDord-b75a6751a95049cb8d4a6eba42d81a6e
Quellennotizuspto-grants-2013_08