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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1026247Generated: November 1, 2026

Azobisisobutyronitrile → HCID 68760715, compound

https://huagongshe.com/reaction/1026247

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
Reactant4-Ethoxy-1-methyl-2-nitrobenzeneHCID 350366—
SolventEthyl AcetateHCID 8857—
ProductHCID 68760715HCID 6876071566.7%

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 4-ethoxy-1-methyl-2-nitrobenzene (11.8 g), N-bromosuccinimide (17.4 g), 2,2′-azobisisobutyronitrile (1.07 g) and ethyl acetate (300 mL) was stirred under an argon atmosphere at 90° C. overnight. The solvent was evaporated under reduced pressure, and the residue was diluted with diethyl ether, and the mixture was washed three times with water. The separated organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound as a yellow oil (11.3 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729102B2
Source datasetuspto-grants-2014_05
ORD IDord-87cfd163d8c74113a7222244c48f9e8a
Source noteuspto-grants-2014_05