HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1890629Generated: October 25, 2026
Azobisisobutyronitrile → 3-(Bromomethyl)benzophenone
https://huagongshe.com/reaction/1890629
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 3-Methylbenzophenone | HCID 69511 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 3-(Bromomethyl)benzophenone | HCID 89586 | 77% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08507484B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-b75a6751a95049cb8d4a6eba42d81a6e |
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| Source note | uspto-grants-2013_08 |
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