HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 241276Erstellt: 25. Oktober 2026
N-bromobutanimide → 3-(Bromomethyl)-6-phenylpyridazine
https://huagongshe.com/reaction/241276
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | N-bromobutanimide | HCID 67184 | — |
| Edukt | 2,2'-Azobis(2,4-dimethylvaleronitrile) | HCID 91537 | — |
| Edukt | 3-Methyl-6-phenylpyridazine | HCID 11378744 | — |
| Lösungsmittel | 1,2-Dichloroethane | HCID 11 | — |
| Produkt | 3-(Bromomethyl)-6-phenylpyridazine | HCID 66717445 | 33,2% |
Reaktionsschritte
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%)
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08648097B2 |
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| Quelldatensatz | uspto-grants-2014_02 |
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| ORD ID | ord-9764fadbf8674d9f85871f740dd60b76 |
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| Quellennotiz | uspto-grants-2014_02 |
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