HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 75554Generated: October 24, 2026
Acetic Acid → (Z)-Ethyl 3-((2-amino-2-oxoethyl)amino)-3-(2-(2-hydroxyethoxy)phenyl)acrylate
https://huagongshe.com/en/reaction/75554
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Glycinamide hydrochloride | HCID 2723639 | — |
| Reactant | Ethyl 3-(2-(2-hydroxyethoxy)phenyl)-3-oxopropanoate | HCID 86684692 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (Z)-Ethyl 3-((2-amino-2-oxoethyl)amino)-3-(2-(2-hydroxyethoxy)phenyl)acrylate | HCID 86684693 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08835449B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-ffdb5ae04a694f5bac5a85efe7d4ce8c |
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| Source note | uspto-grants-2014_09 |
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