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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1890629Generated: October 25, 2026

Azobisisobutyronitrile → 3-(Bromomethyl)benzophenone

https://huagongshe.com/reaction/1890629

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
Reactant3-MethylbenzophenoneHCID 69511—
SolventCarbon TetrachlorideHCID 5943—
Product3-(Bromomethyl)benzophenoneHCID 8958677%

Reaction Conditions

Temperature75 °C

Reaction Steps

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%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507484B2
Source datasetuspto-grants-2013_08
ORD IDord-b75a6751a95049cb8d4a6eba42d81a6e
Source noteuspto-grants-2013_08