Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 256604Generated: October 29, 2026

Azobisisobutyronitrile → HCID 19785591, compound

https://huagongshe.com/reaction/256604

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 19785605HCID 19785605—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 19785591HCID 1978559156%

Reaction Steps

A solution of N-methyl-N-(4-tolyl)methanesulphonamide (0.31 g, 1.54 mmol), N-bromosuccinimide (0.28 g, 1.55 mmol) and 2,2'-azobisisobutyronitrile (20 mg) in carbon tetrachloride (20 ml) was refluxed for 2 hours. The mixture was then cooled to ambient temperature and filtered. The solvent was evaporated and the residue partitioned between ethyl acetate (50 ml) and water (50 ml), washed with brine (50 ml) and dried (MgSO4). The solvent was evaporated yielding N-(4-bromomethylphenyl)-N-methylmethanesulphonamide (0.24 g, 54%) which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05258399
Source datasetuspto-grants-1993_11
ORD IDord-38616543f18141c1a008e0fc407257ff
Source noteuspto-grants-1993_11