Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nabumetone | HCID 4409 | — |
| Reactant | 6-Bromo-2-naphthalenol | HCID 27144 | — |
| Reactant | 2-Bromo-6-methoxynaphthalene | HCID 78786 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-Methoxy-2-naphthaldehyde | HCID 76991 | — |
Reaction Steps
When it is wished to convert the 6-bromo-2-naphthol to nabumetone, the 6-bromo-2-naphthol is first converted to a 6-bromo-2-methoxynaphthalene intermediate as described above, and the intermediate is then converted to nabumetone by any of the techniques already known for that conversion. For example, as described in U.S. Pat. No. 5,225,603 (Aslam et al.), the 6-bromo-2-methoxynaphthalene may be (a) reacted with N,N-dimethylformamide to form 6-methoxy-2-naphthaldehyde, which is then condensed with acetone to prepare a 4-(6-methoxy-2-naphthyl)-3-buten-2-one intermediate that is then catalytically hydrogenated to nabumetone or (b) reacted with methyl vinyl ketone to form the 4-(6-methoxy-2-naphthyl)-3-buten-2-one intermediate that is then catalytically hydrogenated to nabumetone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06121500 |
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| Source dataset | uspto-grants-2000_09 |
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| ORD ID | ord-ffd10bee2f4b412ab13f85c2f39dadfa |
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| Source note | uspto-grants-2000_09 |
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