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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 77553Generated: October 25, 2026

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

https://huagongshe.com/reaction/77553

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantTriethylamineHCID 8471—
ReactantSodium BicarbonateHCID 516892—
ReactantGlycinamide hydrochlorideHCID 2723639—
ReactantEthyl 3-(2-(2-hydroxyethoxy)phenyl)-3-oxopropanoateHCID 86684692—
SolventMethanolHCID 887—
Product(Z)-Ethyl 3-((2-amino-2-oxoethyl)amino)-3-(2-(2-hydroxyethoxy)phenyl)acrylateHCID 86684693—

Reaction Conditions

Temperature40 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841314B2
Source datasetuspto-grants-2014_09
ORD IDord-4d034faaf30a4268be8bac9fe610477f
Source noteuspto-grants-2014_09