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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 412153Generated: October 29, 2026

Azobisisobutyronitrile → HCID 18536041, compound

https://huagongshe.com/reaction/412153

Reaction equation

Participants

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

Reaction Steps

To a solution of the product from Step A (10.38 g, 39.2 mmol) and N-bromosuccinimide (8.61 g, 48.4 mmol) in 80 mL of carbontetrachloride was added 2,2′-azobisisobutyronitrile (0.89 g, 5.4 mmol), and the reaction was heated at reflux overnight under argon. The solution was cooled to room temperature, concentrated in vacuo, slurried with 30% EtOAc/hexane solution, and filtered. The filtrate was washed with saturated aq. NaHCO3 and brine, dried (Na2SO4), filtered, and concentrated in vacuo to provide a 2:1 mixture of the titled product and a tribromide as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06562823B1
Source datasetuspto-grants-2003_05
ORD IDord-fafe44d265b6408d9ad0522c6804d18e
Source noteuspto-grants-2003_05