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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 345034Generated: October 31, 2026

Azobisisobutyronitrile → HCID 18521725, compound

https://huagongshe.com/reaction/345034

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 11/2hours 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 numberUS05055473
Source datasetuspto-grants-1991_10
ORD IDord-68a11246474c4c2c91ad7e597f1e1fae
Source noteuspto-grants-1991_10