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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2212257생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/2212257

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl cyanoacetateHCID 7764—
반응물3-MethylacetophenoneHCID 11455—
반응물Ammonium AcetateHCID 517165—
용매Acetic AcidHCID 176—
용매BenzeneHCID 241—
용매Ethyl AcetateHCID 8857—
생성물2-Cyano-3-(3-methylphenyl)-but-2-enoic acid ethyl esterHCID 297786—

반응 단계

A mixture of 3′-methylacetophenone (50 mmole), ethyl cyanoacetate (50 mmole), 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 mmole), 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 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/petroleum ether. The purified oil solidified on standing at room tempera-ture.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07101905B2
출처 데이터셋uspto-grants-2006_09
ORD IDord-51037baff34b4c6a93219cef0f9aa86f
출처 메모uspto-grants-2006_09