HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1795310Generated: October 25, 2026
Azobisisobutyronitrile → 4-Bromomethylperfluorobiphenyl
https://huagongshe.com/reaction/1795310
Participants
| Role | Name | HCID | Charge |
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| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 4-Methylperfluorobiphenyl | HCID 58782894 | — |
| Product | 4-Bromomethylperfluorobiphenyl | HCID 86591121 | 60% |
Reaction Steps
A mixed solution of a mixture comprising the 4-methylperfluorobiphenyl mentioned above, an N-bromo succinic imide (NBS) (26.7 g, 150 mmol), AIBN (0.99 g, 6 mmol) andacarbon tetrachloride (100 mL) was subjected to heating under reflux for 1 week. During this process, the progress of the reaction was confirmed by TLC, and NBS and AIBN were added on a timely basis. Ultimately, 285 mmol NBS and 15 mmol AIBN were added to the solution. After the reaction was completed, the solution was cooled to room temperature, and the solvent was removed under reduced pressure. The crude product was purified by silica gel column chromatography (developing solvent: hexane-ethyl acetate=100:1), and the 4-(bromomethyl)perfluorobiphenyl (7.36 g, 18 mmol, total yield from methyl lithium 60%) was isolated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07026409B2 |
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| Source dataset | uspto-grants-2006_04 |
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| ORD ID | ord-46bb7ecad4ac430ca08e02b95be2737b |
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| Source note | uspto-grants-2006_04 |
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