HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 992883Generated: October 31, 2026
Azobisisobutyronitrile → HCID 15457079, compound
https://huagongshe.com/reaction/992883
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 15457083 | HCID 15457083 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | HCID 15457079 | HCID 15457079 | 79% |
Reaction Steps
0.98 g (2.72 mmol) of 3-(7-chloro-5-fluoro-2-methylbenzofuran-4-yl)-1-methyl-6-trifluoromethyl-2-(1H)-pyridone was dissolved in 25 ml of carbon tetrachloride, and 0.51 g (2.86 mmol) of NBS and 0.04 g (0.27 mmol) of 2,2′-azobisisobutyronitrile were added thereto, followed by refluxing for 2 hours. Succinic acid imide was removed by filtration. Then, carbon tetrachloride was distilled off under reduced pressure, and the obtained residue was poured into water and extracted with ethyl acetate. After washing with water, the organic layer was dried over anhydrous magnesium sulfate. Ethyl acetate was distilled off under reduced pressure, and the obtained crude crystals were washed with n-hexane to obtain 0.94 g (yield: 79%) of the desired product. Melting point: 142-144° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06472348B1 |
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| Source dataset | uspto-grants-2002_10 |
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| ORD ID | ord-6f6883d36cbe4a258b6be65cba6a2737 |
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| Source note | uspto-grants-2002_10 |
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