Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 241276Erstellt: 25. Oktober 2026

N-bromobutanimide → 3-(Bromomethyl)-6-phenylpyridazine

https://huagongshe.com/reaction/241276

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-bromobutanimideHCID 67184—
Edukt2,2'-Azobis(2,4-dimethylvaleronitrile)HCID 91537—
Edukt3-Methyl-6-phenylpyridazineHCID 11378744—
Lösungsmittel1,2-DichloroethaneHCID 11—
Produkt3-(Bromomethyl)-6-phenylpyridazineHCID 6671744533,2%

Reaktionsbedingungen

Temperatur80 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08648097B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-9764fadbf8674d9f85871f740dd60b76
Quellennotizuspto-grants-2014_02