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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 75556Erstellt: 25. Oktober 2026

Acetic Acid → (Z)-Methyl 3-(2,4-dimethoxyphenyl)-3-((2-ethoxy-2-oxoethyl)amino)acrylate

https://huagongshe.com/reaction/75556

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktTriethylamineHCID 8471—
EduktGlycine methyl ester hydrochlorideHCID 122755—
EduktMethyl 2,4-dimethoxy-beta-oxobenzenepropanoateHCID 2063901—
LösungsmittelEthanolHCID 702—
Produkt(Z)-Methyl 3-(2,4-dimethoxyphenyl)-3-((2-ethoxy-2-oxoethyl)amino)acrylateHCID 8668469569,2%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

To a solution of methyl 3-(2,4-dimethoxyphenyl)-3-oxopropanoate (5.0 g, 21 mmol) in EtOH (30 mL) was added glycine methyl ester hydrochloride (10.5 g, 83.9 mmol) followed by acetic acid (1.20 mL, 21 mmol) and triethylamine (8.5 g, 83.9 mmol) and the reaction mixture was heated at 100° C. for 18 hours. After cooling to room temperature, the residue was partitioned between EtOAc and saturated aqueous ammonium chloride. The organic layer was washed with brine, dried over sodium sulfate and concentrated in vacuo. The crude product was dissolved in CH2Cl2 (10 mL) filtered through a plug of silica gel, eluting with 15-35% EtOAc in heptanes and dried under vacuum to give the title compound (4.7 g, 69%) as a yellow solid. This material was used in the next step without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08835449B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-9921a0d60d1748beb999e57d661a0712
Quellennotizuspto-grants-2014_09