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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 436672Generated: October 26, 2026

2-Acetylnaphthalene → 2-Naphthoic acid

https://huagongshe.com/reaction/436672

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AcetylnaphthaleneHCID 7122—
Reactant2-Naphthoic acidHCID 7123—
ReactantDiboronHCID 6328200—
ReactantSodium HypochloriteHCID 23665760—
SolventDiethyl EtherHCID 3283—
SolventDiglymeHCID 8150—
Product2-Naphthoic acidHCID 7123—
Product2-NaphthalenemethanolHCID 74128—

Reaction Steps

2-Acetylnaphthalene is prepared by treating 2-(1-bromoethyl)naphthalene, prepared as described above, with sodium acetate in acetic acid to afford 2-(1-acetoxyethyl)naphthalene which upon base hydrolysis furnishes the 2-(1-hydroxyethyl)naphthalene. The latter is oxidized with an equivalent of chromium trioxide in glacial acetic acid, or 8N sulfuric acid and acetone to furnish 2-acetylnaphthalene. 2-Carboxynaphthalene is prepared from 2-acetylnaphthalene by treating the latter with aqueous sodium hypochlorite. The 2-carboxynaphthalene is treated with diborane in an ether, such as diglyme (diethyleneglycol dimethyl ether), to yield 2-hydroxymethylnaphthalene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04009197
Source datasetuspto-grants-1977_02
ORD IDord-fee330c163c5406791381ec023d45b83
Source noteuspto-grants-1977_02