HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250320Generated: October 30, 2026
Azobisisobutyronitrile → 7-(Bromomethyl)-2-naphthonitrile
https://huagongshe.com/reaction/1250320
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 7-Methyl-2-naphthalenecarbonitrile | HCID 9815323 | — |
| Solvent | Isobutyronitrile | HCID 6559 | — |
| Product | 7-(Bromomethyl)-2-naphthonitrile | HCID 9837748 | 58.2% |
Reaction Steps
2,2′-azobisisobutyronitrile (491 mg, 3 mmol) and isobutyronitrile (50 ml) were added to 7-methyl-2-naphthalene carbonitrile (5.0 g, 30 mmol) at room temperature. N-bromosuccinimide (5.3 g, 30 mmol) was added thereto, and the mixture was heated at an internal temperature of 80° C. for 2 hours. After that, the experiment was conducted in the same way as Example 12. Analysis by reversed-phase chromatography by use of the obtained product from Example 11 as a standard sample revealed that 4.3 g of the title compound was obtained (58% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06337405B1 |
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| Source dataset | uspto-grants-2002_01 |
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| ORD ID | ord-8d09dd0b37fb4f469c8ffc1757535b7b |
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| Source note | uspto-grants-2002_01 |
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