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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1889373Generated: November 2, 2026

Azobisisobutyronitrile → HCID 59351659, compound

https://huagongshe.com/reaction/1889373

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 59351792HCID 59351792—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 59351659HCID 5935165953.1%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 4-[(2-methoxyethoxy)methyl]-3-(4′-methylbiphenyl-2-yl)-1,2,4-oxadiazol-5(4H)-one (46.6 g), N-bromosuccinimide (26.9 g), α,α′-azobisisobutyronitrile (2.2 g) and carbon tetrachloride (500 mL) was stirred at 80° C. for 6 hr. Insoluble material was filtered off, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography to give the title compound as colorless oil (30.5 g, 53%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501750B2
Source datasetuspto-grants-2013_08
ORD IDord-476b5ca6ca9847fbbeb66c4210d65a01
Source noteuspto-grants-2013_08