HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 241276Generated: October 25, 2026
N-bromobutanimide → 3-(Bromomethyl)-6-phenylpyridazine
https://huagongshe.com/reaction/241276
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2,2'-Azobis(2,4-dimethylvaleronitrile) | HCID 91537 | — |
| Reactant | 3-Methyl-6-phenylpyridazine | HCID 11378744 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 3-(Bromomethyl)-6-phenylpyridazine | HCID 66717445 | 33.2% |
Reaction Steps
To a solution of 3-methyl-6-phenylpyridazine (925 mg, 5.43 mmol) in 1,2-dichloroethane (28 ml) were added NBS (1.07 g, 6.01 mmol) and 2,2′-azobis(2,4-dimethylvaleronitrile) (67.3 mg, 0.271 mmol), followed by stirring at 80° C. for 1 hour. During the reaction, 2,2′-azobis(2,4-dimethylvaleronitrile)(134 mg, 0.540 mmol) was additionally added in two portions. After completion of the reaction, the reaction solution was concentrated under reduced pressure. The resulting residue was subjected to silica gel column chromatography (eluent; hexane:ethyl acetate=5:1→0:1 (V/V)), and fractions containing the desired compound were concentrated under reduced pressure to afford the title compound (449 mg) as a slightly brown solid. (Yield: 33%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08648097B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-9764fadbf8674d9f85871f740dd60b76 |
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| Source note | uspto-grants-2014_02 |
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