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HRID 1743035作成日:2026年10月27日

Methanesulfonic Acid → 1-(4-Pyridyl)-2,3-bis(methoxycarbonyl)-6,7-dimethoxynaphthalene

https://huagongshe.com/reaction/1743035

反応式

関与物質

役割名称HCID仕込み量
反応物Methanesulfonic AcidHCID 6395—
反応物Dimethyl maleateHCID 5271565—
反応物3,4-Dimethoxy-6-(4-pyridyl) hydroxymethylbenzaldehyde dimethylacetalHCID 22007378—
溶媒Acetic AcidHCID 176—
溶媒TolueneHCID 1140—
生成物1-(4-Pyridyl)-2,3-bis(methoxycarbonyl)-6,7-dimethoxynaphthaleneHCID 1172864262.2%

反応手順

To a solution of 3,4-dimethoxy-6-(4-pyridyl) hydroxymethylbenzaldehyde dimethylacetal (18.4 g) in a mixture of acetic acid (50 ml) and toluene (50 ml) is added dimethyl maleate (8.64 ml), and the mixture is refluxed for one hour. To the mixture is added methanesulfonic acid (9.33 ml), and the mixture is refluxed for 8 hours while removing the resulting water with a Dean-Stalk apparatus. The mixture is cooled to room temperature, and concentrated. The residue is dissolved in chloroform, and the pH value thereof is adjusted with aqueous potassium carbonate solution to pH 8. The mixture is extracted twice with each 100 ml of chloroform, and the extracts are washed with a saturated sodium chloride solution, dried over magnesium sulfate, and concentrated. The resulting residue is crystallized from diethyl ether to give a diester compound, 1-(4-pyridyl)-2,3-bis(methoxycarbonyl)-6,7-dimethoxynaphthalene (13.5 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05342941
出典データセットuspto-grants-1994_08
ORD IDord-ea6e579a5bde40b8844841c48e68995a
出典メモuspto-grants-1994_08