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HRID 477337作成日:2026年10月23日

Sodium ethoxide → Ethyl 2-dimethylamino-5-methylthio-6-(2-naphthyl)-6-oxo-2,4-hexadienoate

https://huagongshe.com/ja/reaction/477337

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium ethoxideHCID 2723922—
反応物2-[2-(Methylthio)acetyl]naphthaleneHCID 15833815—
反応物Ethyl 6-phenyl-6-oxo-5-methylthio-2-dimethylamino2,4-hexadienoateHCID 44325574—
反応物N-(dimethylamino-3-ethoxycarbonylpropenylidene)-N-methylmethanaminium tetrafluoroborateHCID 86743575—
溶媒EthanolHCID 702—
生成物Ethyl 2-dimethylamino-5-methylthio-6-(2-naphthyl)-6-oxo-2,4-hexadienoateHCID 54464034—

反応手順

The procedure is as in Example 4 for the preparation of ethyl 6-phenyl-6-oxo-5-methylthio-2-dimethylamino-2,4-hexadienoate, starting with N-(3-dimethylamino-3-ethoxycarbonylpropenylidene)-N-methylmethanaminium tetrafluoroborate (10.6 g), a 2M ethanolic solution of sodium ethylate (18.5 cc) and 2-[2-(methylthio)acetyl]naphthalene (8 g) in ethanol (50 cc). After purification by chromatography on a silica column with a mixture of cyclohexane and ethyl acetate (50:50 by volume) as eluent, ethyl 2-dimethylamino-5-methylthio-6-(2-naphthyl)-6-oxo-2,4-hexadienoate (5 g) is obtained in the form of an orange-coloured oil, and is used in the crude state in the subsequent syntheses.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04886835
出典データセットuspto-grants-1989_12
ORD IDord-ced127c0353947eca800723ad5a9ae6d
出典メモuspto-grants-1989_12