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HRID 270196作成日:2026年10月27日

Ethyl cyanoacetate → Ethyl 2-cyano-3-[3-(methyloxy)phenyl]-2-butenoate

https://huagongshe.com/reaction/270196

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-MethoxyacetophenoneHCID 11460—
反応物Ammonium AcetateHCID 517165—
溶媒Acetic AcidHCID 176—
溶媒BenzeneHCID 241—
溶媒Ethyl AcetateHCID 8857—
生成物Ethyl 2-cyano-3-[3-(methyloxy)phenyl]-2-butenoateHCID 4115002—

反応手順

A mixture of 3′-methoxyacetophenone (50 mmol), ethyl cyanoacetate (50 mmol), acetic acid (1.14 mL) ammonium acetate (400 mg), and benzene (50 mL) is 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 is cooled to room temperature, diluted with ethyl acetate (30 mL), washed with water (240 mL), brine (40 mL), and dried (Na2SO4). After filtering, the extract is concentrated in vacuo and the desired product, as a mixture of E and Z-isomers, is isolated by column chromatography on silica gel, eluting with 5% ethyl acetate in petroleum ether.

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-3d2af61ac6fd43fbab984afda5b201a9
出典メモuspto-grants-2008_11