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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1954498Generated: November 2, 2026

Ethylene → 2-Vinyl-6-methoxynaphthalene

https://huagongshe.com/reaction/1954498

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyleneHCID 6325—
Reactant6-Bromo-2-naphthalenolHCID 27144—
Reactant2-Bromo-6-methoxynaphthaleneHCID 78786—
ReactantNaproxenHCID 156391—
Product2-Vinyl-6-methoxynaphthaleneHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06121500
Source datasetuspto-grants-2000_09
ORD IDord-574962bf6f8e4d5eb4b6b6abd0bbe25f
Source noteuspto-grants-2000_09