Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2306227Generated: November 3, 2026

Azobisisobutyronitrile → HCID 18536041, compound

https://huagongshe.com/reaction/2306227

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 18536178HCID 18536178—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 18536041HCID 18536041—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of methanesulfonic acid 4-bromo-3-methylphenyl ester, as described above in Step B, (14.3 g, 53.9 mmol), N-bromosuccinimide (14.4 g, 80.9 mmol), and 2,2′-azobisisobutyronitrile (1.34 g, 8.16 mmol) in CCl4 was heated at 80° C. for 18 hours. The solvent was removed under reduced pressure and the residue was purified by silica gel chromatography, eluting with a gradient of hexane—5% to 20% EtOAc, to yield the titled product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06441017B1
Source datasetuspto-grants-2002_08
ORD IDord-31c3f441d8e84cf4bf2ed2b4e671501e
Source noteuspto-grants-2002_08