HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2091041Generated: October 31, 2026
Azobisisobutyronitrile → HCID 66778012, compound
https://huagongshe.com/reaction/2091041
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 16433918 | HCID 16433918 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 66778012 | HCID 66778012 | 71.1% |
Reaction Steps
To a solution (150 mL) of methyl 5-fluoro-3-methyl-1-benzofuran-2-carboxylate (15.4 g) synthesized above in acetonitrile were added N-bromosuccinimide (19.8 g) and 2,2′-azobis(isobutyronitrile) (1.21 g), and the mixture was stirred under argon atmosphere at 50° C. for 2.5 days. The reaction mixture was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (20-30% ethyl acetate/hexane) to give a white solid. The obtained solid was washed with hexane to give the title object compound (15.1 g, 71%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08436043B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-7dd68d411ba64cd4a507be06ffe86142 |
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| Source note | uspto-grants-2013_05 |
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