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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1061872Generated: November 1, 2026

Azobisisobutyronitrile → HCID 22285068, compound

https://huagongshe.com/reaction/1061872

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 22285057HCID 22285057—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 22285068HCID 2228506899.5%

Reaction Steps

Methyl 6-[1-hydroxy-2-methyl-1-(1-trityl-1H-imidazol-4-yl)propyl]-3-methyl-2-naphthoate (5.93 g) was suspended in carbon tetrachloride (150 ml) and N-bromosuccinimide (2.01 g) and 2,2′-azobisisobutyronitrile (0.17 g) were added. The reaction mixture was heated under reflux for 4 hrs. and the solvent was concentrated. The residue was diluted with saturated aqueous sodium hydrogen carbonate and extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and concentrated to give a crude title compound (6.70 g) as a brown amorphous solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06960586B2
Source datasetuspto-grants-2005_11
ORD IDord-ce2a0861c6e445eb8c7b4d7b80054ae4
Source noteuspto-grants-2005_11