HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 77553Erstellt: 24. Oktober 2026
Acetic Acid → (Z)-Ethyl 3-((2-amino-2-oxoethyl)amino)-3-(2-(2-hydroxyethoxy)phenyl)acrylate
https://huagongshe.com/de/reaction/77553
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | Glycinamide hydrochloride | HCID 2723639 | — |
| Edukt | Ethyl 3-(2-(2-hydroxyethoxy)phenyl)-3-oxopropanoate | HCID 86684692 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | (Z)-Ethyl 3-((2-amino-2-oxoethyl)amino)-3-(2-(2-hydroxyethoxy)phenyl)acrylate | HCID 86684693 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US08841314B2 |
|---|
| Quelldatensatz | uspto-grants-2014_09 |
|---|
| ORD ID | ord-4d034faaf30a4268be8bac9fe610477f |
|---|
| Quellennotiz | uspto-grants-2014_09 |
|---|