HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1026247Generated: November 1, 2026
Azobisisobutyronitrile → HCID 68760715, compound
https://huagongshe.com/reaction/1026247
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 4-Ethoxy-1-methyl-2-nitrobenzene | HCID 350366 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 68760715 | HCID 68760715 | 66.7% |
Reaction Steps
A mixture of 4-ethoxy-1-methyl-2-nitrobenzene (11.8 g), N-bromosuccinimide (17.4 g), 2,2′-azobisisobutyronitrile (1.07 g) and ethyl acetate (300 mL) was stirred under an argon atmosphere at 90° C. overnight. The solvent was evaporated under reduced pressure, and the residue was diluted with diethyl ether, and the mixture was washed three times with water. The separated organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound as a yellow oil (11.3 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08729102B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-87cfd163d8c74113a7222244c48f9e8a |
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| Source note | uspto-grants-2014_05 |
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