戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 477330作成日:2026年10月26日

2-Methoxy-1-phenylethanone → Ethyl 2-dimethylamino-5-methoxy-6-oxo-6-phenyl-2,4-hexadienoate

https://huagongshe.com/reaction/477330

反応式

関与物質

役割名称HCID仕込み量
反応物2-Methoxy-1-phenylethanoneHCID 77698—
反応物Sodium ethoxideHCID 2723922—
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-methoxy-6-oxo-6-phenyl-2,4-hexadienoateHCID 53661101—

反応手順

The procedure is as in Example 4 for the preparation of ethyl 6-phenyl-6-oxo-5-methylthio-2-dimethylamino2,4-hexadienoate, starting with N-(3-dimethylamino-3-ethoxycarbonylpropenylidene)-N-methylmethanaminium tetrafluoroborate (11.4 g), a 2M ethanolic solution of sodium ethylate (20 cc) and α-methoxyacetophenone (6 g) in ethanol (50 cc). After purification by chromatography on a silica column with a mixture of dicholoromethane and ethyl acetate (50:50 by volume) as eluent, ethyl 2-dimethylamino-5-methoxy-6-oxo-6-phenyl-2,4-hexadienoate (8.1 g) is obtained, 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-6e6464c9218943b8abb6cc76a80a7f64
出典メモuspto-grants-1989_12