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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 241276Generated: October 25, 2026

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

https://huagongshe.com/reaction/241276

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant2,2'-Azobis(2,4-dimethylvaleronitrile)HCID 91537—
Reactant3-Methyl-6-phenylpyridazineHCID 11378744—
Solvent1,2-DichloroethaneHCID 11—
Product3-(Bromomethyl)-6-phenylpyridazineHCID 6671744533.2%

Reaction Conditions

Temperature80 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08648097B2
Source datasetuspto-grants-2014_02
ORD IDord-9764fadbf8674d9f85871f740dd60b76
Source noteuspto-grants-2014_02