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HRID 2212287作成日:2026年10月25日

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

https://huagongshe.com/reaction/2212287

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 mmole), ethyl cyanoacetate (50 mmole), 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 mmole), 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/petroleum ether.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07101905B2
出典データセットuspto-grants-2006_09
ORD IDord-5f9e5946f1734296a7c1a59c9af2489c
出典メモuspto-grants-2006_09