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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1506148Generated: October 31, 2026

Azobisisobutyronitrile → HCID 86726615, compound

https://huagongshe.com/reaction/1506148

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
Reactant5-Methyl-2-(trifluoromethyl)benzonitrileHCID 17750725—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 86726615HCID 8672661549.1%

Reaction Steps

5-Methyl-2-(trifluoromethyl)benzonitrile (200 mg, 1.08 mmol) in 1,2-dichloroethane (3 mL) was stirred with N-bromosuccinimide (192 mg, 1.08 mmol) and azobisisobutyronitrile (36.1 mg, 0.22 mmol) at 80° C. for 2 hours. The reaction mixture allowed to cool to room temperature and was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane→ethyl acetate/hexane=1/3 (v/v)) to give the title compound as a colorless solid (140 mg, yield 49%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216999B2
Source datasetuspto-grants-2015_12
ORD IDord-1f915a0d7c904efa9360c440c07c214d
Source noteuspto-grants-2015_12