HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1761880Generated: October 29, 2026
Azobisisobutyronitrile → HCID 18521725, compound
https://huagongshe.com/reaction/1761880
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2-Methyl-6-nitro-1-benzofuran | HCID 13170310 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | HCID 18521725 | HCID 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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04829071 |
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| Source dataset | uspto-grants-1989_05 |
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| ORD ID | ord-bef1bd937ce94d91971841cbb75bbdc7 |
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| Source note | uspto-grants-1989_05 |
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