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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 467092Generated: October 30, 2026

Azobisisobutyronitrile → HCID 18521725, compound

https://huagongshe.com/reaction/467092

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
Reactant2-Methyl-6-nitro-1-benzofuranHCID 13170310—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 18521725HCID 18521725—

Reaction Steps

N-Bromosuccinimide ("NBS") (1.11 g, 6.2 mmole) was added to a solution of 2-methyl-6-nitrobenzofuran (1.00 g, 5.65 mmole) and azobisisobutyronitrile (20 mg) in carbon tetrachloride and the mixture was heated at reflux temperature for 11/2 hours in the presence of a bright light. The solvent was then evaporated and the residue dissolved in methylene chloride, washed with water, dried (MgSO4), evaporated to dryness and purified by column chromatography on silica eluting with methylene chloride/hexane (7:3). The product-containing fractions were combined and evaporated to give the title compound, yield 1.43 g. 'H-N.m.r. clearly showed that the product contained 20% of 2-dibromomethyl-6-nitrobenzofuran, however, it was not considered necessary to remove this and the product was used directly without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05158964
Source datasetuspto-grants-1992_10
ORD IDord-df5f97d22f05436eab81e04e12a35fd8
Source noteuspto-grants-1992_10