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HRID 649591作成日:2026年10月24日

Water → diethyl N-(4-ethylcyclohexen-1-yl)-aminomethylenemalonate

https://huagongshe.com/ja/reaction/649591

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物p-Toluenesulfonic acidHCID 6101—
反応物4-EthylcyclohexanoneHCID 79506—
反応物Diethyl (aminomethylidene)propanedioateHCID 226751—
溶媒TolueneHCID 1140—
生成物diethyl N-(4-ethylcyclohexen-1-yl)-aminomethylenemalonateHCID 14153004—

反応手順

A mixture of 12.6 g of 4-ethylcyclohexanone, 17.0 g of diethyl aminomethylenemalonate, and 950 mg of p-toluenesulfonic acid in 170 ml of toluene is heated at reflux for 48 hours with a water separator, under nitrogen atmosphere. The solvent is removed under nitrogen atmosphere and under vacuum, and the residue purified by flash column chromatooraphy on a silica qel column eluted with methylene chloride. The desired product, diethyl N-(4-ethylcyclohexen-1-yl)-aminomethylenemalonate is obtained as an oil. The purified product in 90 ml Dowtherm is aded to 300 ml Dowtherm preheated to 250° under nitrogen atmosphere. After heating at 240°-245° for 4 hours the reaction mixture is cooled and allowed to stand at room temperature overnight. The precipitate which formed is filtered off, washed with hexane and air-dried. Recrystallization form isopropanol after treatment with decolorizing carbon affords ethyl 4-hydroxy-6-ethyl-5,6,7,8-tetrahydroquinoline-3-carboxylate m.p. 218°-220°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04740512
出典データセットuspto-grants-1988_04
ORD IDord-d10468cb8acb40e2bd82b66e43989ade
出典メモuspto-grants-1988_04