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HRID 77553作成日:2026年10月24日

Acetic Acid → (Z)-Ethyl 3-((2-amino-2-oxoethyl)amino)-3-(2-(2-hydroxyethoxy)phenyl)acrylate

https://huagongshe.com/ja/reaction/77553

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Sodium BicarbonateHCID 516892—
反応物Glycinamide hydrochlorideHCID 2723639—
反応物Ethyl 3-(2-(2-hydroxyethoxy)phenyl)-3-oxopropanoateHCID 86684692—
溶媒MethanolHCID 887—
生成物(Z)-Ethyl 3-((2-amino-2-oxoethyl)amino)-3-(2-(2-hydroxyethoxy)phenyl)acrylateHCID 86684693—

反応条件

温度40 °C

反応手順

To a solution of ethyl 3-(2-(2-hydroxyethoxy)phenyl)-3-oxopropanoate (2 g, 7.94 mmol) and glycinamide hydrochloride (3.5 g, 31.7 mmol) in methanol (20 mL) was added triethylamine (3.21 g, 31.7 mmol) at room temperature. The mixture was stirred at 40° C. for 20 min. Acetic acid (1.9 g, 31.7 mmol) was added, and the mixture was stirred at 80° C. for 18 hours. The reaction mixture was cooled to room temperature and saturated sodium bicarbonate (200 mL) was added. The organic layer was separated, dried (Na2SO4) and concentrated to give a yellow solid. The solid was washed with EtOAc (20 mL), and the residue was dried under reduced pressure to give the title compound as a white solid. This material was used 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-4d034faaf30a4268be8bac9fe610477f
出典メモuspto-grants-2014_09