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HRID 77555作成日:2026年10月25日

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

https://huagongshe.com/reaction/77555

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物TriethylamineHCID 8471—
反応物Glycine methyl ester hydrochlorideHCID 122755—
反応物Methyl 2,4-dimethoxy-beta-oxobenzenepropanoateHCID 2063901—
溶媒EthanolHCID 702—
生成物(Z)-Methyl 3-(2,4-dimethoxyphenyl)-3-((2-ethoxy-2-oxoethyl)amino)acrylateHCID 8668469569.2%

反応条件

温度100 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08841314B2
出典データセットuspto-grants-2014_09
ORD IDord-76296017362c45adaddc6fda450d4019
出典メモuspto-grants-2014_09