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HRID 436672作成日:2026年10月25日

2-Acetylnaphthalene → 2-Naphthoic acid

https://huagongshe.com/reaction/436672

反応式

関与物質

役割名称HCID仕込み量
反応物2-AcetylnaphthaleneHCID 7122—
反応物2-Naphthoic acidHCID 7123—
反応物DiboronHCID 6328200—
反応物Sodium HypochloriteHCID 23665760—
溶媒Diethyl EtherHCID 3283—
溶媒DiglymeHCID 8150—
生成物2-Naphthoic acidHCID 7123—
生成物2-NaphthalenemethanolHCID 74128—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04009197
出典データセットuspto-grants-1977_02
ORD IDord-fee330c163c5406791381ec023d45b83
出典メモuspto-grants-1977_02