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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1054111Generated: October 25, 2026

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

https://huagongshe.com/reaction/1054111

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant3-Methyl-6-phenylpyridazineHCID 11378744—
SolventCarbon TetrachlorideHCID 5943—
Product3-(Bromomethyl)-6-phenylpyridazineHCID 66717445—

Reaction Steps

Synthesized using compound 65b (982 mg, 5.77 mmol), NBS (1.13 g, 6.35 mmol) and DBPO (70 mg, 0.29 mmol) in carbon tetrachloride according to Method A. Crude product was purified by flash chromatography on silica-gel using hexane/ethyl acetate (4:1) as eluent. Product was used directly in the next step without further characterization. Orange solid. Yield: 53 mg, 4%. (ESI): m/z=250.67 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394290B2
Source datasetuspto-grants-2016_07
ORD IDord-e12083880c59418886cef06b3e62e0f5
Source noteuspto-grants-2016_07