HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1889373Generated: November 2, 2026
Azobisisobutyronitrile → HCID 59351659, compound
https://huagongshe.com/reaction/1889373
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 59351792 | HCID 59351792 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | HCID 59351659 | HCID 59351659 | 53.1% |
Reaction Steps
A mixture of 4-[(2-methoxyethoxy)methyl]-3-(4′-methylbiphenyl-2-yl)-1,2,4-oxadiazol-5(4H)-one (46.6 g), N-bromosuccinimide (26.9 g), α,α′-azobisisobutyronitrile (2.2 g) and carbon tetrachloride (500 mL) was stirred at 80° C. for 6 hr. Insoluble material was filtered off, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography to give the title compound as colorless oil (30.5 g, 53%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08501750B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-476b5ca6ca9847fbbeb66c4210d65a01 |
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| Source note | uspto-grants-2013_08 |
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