HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylene → 2-Vinyl-6-methoxynaphthalene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylene | HCID 6325 | — |
| Reactant | 6-Bromo-2-naphthalenol | HCID 27144 | — |
| Reactant | 2-Bromo-6-methoxynaphthalene | HCID 78786 | — |
| Reactant | Naproxen | HCID 156391 | — |
| Product | 2-Vinyl-6-methoxynaphthalene | HCID 603535 | — |
Reaction Steps
When it is desired to convert the 6-bromo-2-naphthol to naproxen, 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 naproxen by any of the techniques already known for that conversion. For example, as disclosed in U.S. Pat. No. 5,536,870 (Wu), the 6-bromo-2-methoxynaphthalene may be reacted with ethylene to form 2-methoxy-6-vinylnapthalene, which is then carbonylated to racemic 2-(6-methoxy-2-naphthyl)propionic acid, which can be subsequently resolved to isolate the desired naproxen enantiomer.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06121500 |
| Source dataset | uspto-grants-2000_09 |
| ORD ID | ord-574962bf6f8e4d5eb4b6b6abd0bbe25f |
| Source note | uspto-grants-2000_09 |