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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1731064Generated: October 31, 2026

1-Bromo-2-methoxynaphthalene → 1-(5-Bromo-6-methoxynaphthalen-2-yl)ethan-1-one

https://huagongshe.com/reaction/1731064

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-2-methoxynaphthaleneHCID 72860—
Reactant1-Chloro-2-methoxynaphthaleneHCID 11564623—
Reactant1-Fluoro-2-methoxynaphthaleneHCID 12656105—
Product1-(5-Bromo-6-methoxynaphthalen-2-yl)ethan-1-oneHCID 622178—
Product1-(5-Chloro-6-methoxynaphthalen-2-yl)ethan-1-oneHCID 15890459—
ProductHCID 21494953HCID 21494953—

Reaction Steps

Repeating this procedure but replacing the nitrobenzene with dichloromethylene and replacing the β-naphthol methyl ether with 1-bromo-2-methoxynaphthalene, 1-chloro-2-methoxynaphthalene, and 1-fluoro-2-methoxynaphthalene -- 5-bromo-6-methoxy-2-acetylnaphthalene, 5-chloro-6-methoxy-2-acetylnaphthalene, and 5-fluoro-6-methoxy-2-acetylnaphthalene, respectively, were produced. A higher yield was obtained starting with the halo compounds, and less extensive processing was required to obtain a product having high purity.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03994968
Source datasetuspto-grants-1976_11
ORD IDord-1aa941ca6e6b41a5a17c2d1dfde4b570
Source noteuspto-grants-1976_11