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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 75556생성일: 2026년 10월 24일

Acetic Acid → (Z)-Methyl 3-(2,4-dimethoxyphenyl)-3-((2-ethoxy-2-oxoethyl)amino)acrylate

https://huagongshe.com/ko/reaction/75556

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물TriethylamineHCID 8471—
반응물Glycine methyl ester hydrochlorideHCID 122755—
반응물Methyl 2,4-dimethoxy-beta-oxobenzenepropanoateHCID 2063901—
용매EthanolHCID 702—
생성물(Z)-Methyl 3-(2,4-dimethoxyphenyl)-3-((2-ethoxy-2-oxoethyl)amino)acrylateHCID 8668469569.2%

반응 조건

온도100 °C

반응 단계

To a solution of methyl 3-(2,4-dimethoxyphenyl)-3-oxopropanoate (5.0 g, 21 mmol) in EtOH (30 mL) was added glycine methyl ester hydrochloride (10.5 g, 83.9 mmol) followed by acetic acid (1.20 mL, 21 mmol) and triethylamine (8.5 g, 83.9 mmol) and the reaction mixture was heated at 100° C. for 18 hours. After cooling to room temperature, the residue was partitioned between EtOAc and saturated aqueous ammonium chloride. The organic layer was washed with brine, dried over sodium sulfate and concentrated in vacuo. The crude product was dissolved in CH2Cl2 (10 mL) filtered through a plug of silica gel, eluting with 15-35% EtOAc in heptanes and dried under vacuum to give the title compound (4.7 g, 69%) as a yellow solid. This material was used in the next step without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08835449B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-9921a0d60d1748beb999e57d661a0712
출처 메모uspto-grants-2014_09