戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 270166作成日:2026年10月27日

Ethyl cyanoacetate → 2-Cyano-3-(3-methylphenyl)-but-2-enoic acid ethyl ester

https://huagongshe.com/reaction/270166

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl cyanoacetateHCID 7764—
反応物3-MethylacetophenoneHCID 11455—
反応物Ammonium AcetateHCID 517165—
溶媒Acetic AcidHCID 176—
溶媒BenzeneHCID 241—
溶媒Ethyl AcetateHCID 8857—
生成物2-Cyano-3-(3-methylphenyl)-but-2-enoic acid ethyl esterHCID 297786—

反応手順

A mixture of 3′-methylacetophenone (50 mmol), ethyl cyanoacetate (50 mmol), 25 acetic acid (1.14 mL) ammonium acetate (400 mg), and benzene (50 mL) was heated to reflux in a Dean-Stark apparatus. After approximately 10 hours, additional ethyl cyanoacetate (50 mmol), acetic acid (1.14 mL), and ammonium acetate (400 mg) are added. After an additional 10 hours, the reaction was cooled to room temperature, diluted with ethyl acetate (30 mL), washed with water (240 mL), brine (40 mL), and 30 dried (Na2SO4). After filtering, the extract was concentrated in vacuo and the desired product, as a mixture of E and Z-isomers, was isolated by column chromatography on silica gel, eluting with 5% ethyl acetate in petroleum ether. The purified oil solidified on standing at room temperature.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07449490B2
出典データセットuspto-grants-2008_11
ORD IDord-f2ec646ed84c45559c6caa01c5677804
出典メモuspto-grants-2008_11