HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1292830Generated: October 30, 2026
Azobisisobutyronitrile → HCID 17862884, compound
https://huagongshe.com/reaction/1292830
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 3-Bromo-2-methyl-1-benzofuran | HCID 11514006 | — |
| Solvent | Chlorobenzene | HCID 7964 | — |
| Product | HCID 17862884 | HCID 17862884 | 79% |
Reaction Steps
2.7 g (15.3 mmoles) of N-bromosuccinimide and 0.4 g (2.7 mmoles) of azobisisobutyronitrile were added to a solution of 2.8 g (13.3 mmoles) of 3-bromo-2-mehtylbenzofuran dissolved in 30 ml of monochlorobenzene. The mixture was stirred at 80° C. for 30 minutes to give rise to a reaction. After confirmation of the disappearance of the raw materials, the reaction mixture was cooled to room temperature. The insolubles were removed by filtration. The filtrate was subjected to vacuum distillation to remove the solvent contained therein. The residue was poured into water, followed by extraction with ethyl acetate. The resulting organic layer was washed with water and an aqueous sodium chloride solution in this order and then dried over anhydrous magnesium sulfate. The resulting solution was subjected to vacuum distillation to remove the solvent contained therein, to obtain 3.0 g (yield: 79.0%) of 3-bromo-2-bromomethylbenzofuran.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07238689B2 |
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| Source dataset | uspto-grants-2007_07 |
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| ORD ID | ord-ac5833376fcb4529a0c467514b133595 |
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| Source note | uspto-grants-2007_07 |
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