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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2254663Generated: November 1, 2026

Azobisisobutyronitrile → HCID 19785591, compound

https://huagongshe.com/reaction/2254663

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 numberUS05236948
Source datasetuspto-grants-1993_08
ORD IDord-cc1555d60e7b43d5868d36aea75bd33b
Source noteuspto-grants-1993_08