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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 75554Erstellt: 23. Oktober 2026

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

https://huagongshe.com/de/reaction/75554

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktTriethylamineHCID 8471—
EduktSodium BicarbonateHCID 516892—
EduktGlycinamide hydrochlorideHCID 2723639—
EduktEthyl 3-(2-(2-hydroxyethoxy)phenyl)-3-oxopropanoateHCID 86684692—
LösungsmittelMethanolHCID 887—
Produkt(Z)-Ethyl 3-((2-amino-2-oxoethyl)amino)-3-(2-(2-hydroxyethoxy)phenyl)acrylateHCID 86684693—

Reaktionsbedingungen

Temperatur40 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08835449B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-ffdb5ae04a694f5bac5a85efe7d4ce8c
Quellennotizuspto-grants-2014_09