HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1055408Generated: November 1, 2026
Azobisisobutyronitrile → HCID 90037979, compound
https://huagongshe.com/reaction/1055408
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 90037108 | HCID 90037108 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | HCID 90037979 | HCID 90037979 | 38.9% |
Reaction Steps
2,2′-Azobis(2-methylpropionitrile) (AIBN, 17.2 mg, 0.105 mmol) and N-bromosuccinimide (NBS, 97.7 mg, 0.549 mmol) were added to a suspension of 6-fluoro-1,4-dimethylquinolin-2(1H)-one (100 mg, 0.523 mmol) in CCl4 (10 mL) at 70° C. After 1 h an additional 2 eq. of NBS and 0.4 eq. of AIBN were added and the mixture heated at 70° C. for 1 h. The mixture was concentrated and the residue purified by preparative TLC to give desired the title compound (55 mg, 31%) as white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09394263B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-690a0d36dda6407fb3731d9c987b6988 |
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| Source note | uspto-grants-2016_07 |
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