Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 23136528 | HCID 23136528 | — |
| Catalyst | Azobisisobutyronitrile | HCID 6547 | — |
| Solvent | (Trifluoromethyl)benzene | HCID 7368 | — |
| Product | HCID 23136352 | HCID 23136352 | 73.1% |
Reaction Steps
1-(3-Methylphenoxy)naphthalene (500 mg, 2.1 mmol) was dissolved in benzotrifluoride (30 mL), N-bromosuccinimide (417 mg, 2.3 mmol) and 2,2′-azobis(isobutyronitrile) (10 mg, 0.06 mmol) were added thereto, and then the mixture was stirred at 100° C. for 4 hours. The reaction solution was filtered, and concentrated under reduced pressure. The residue was purified with silica gel column chromatography (hexane/ethyl acetate=100:0 to 90:10) to give the title compound (481 mg, yield 73%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08008525B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-51593668d15240359f448e039e59377a |
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| Source note | uspto-grants-2011_08 |
|---|