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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 75556Generated: October 26, 2026

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

https://huagongshe.com/reaction/75556

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantTriethylamineHCID 8471—
ReactantGlycine methyl ester hydrochlorideHCID 122755—
ReactantMethyl 2,4-dimethoxy-beta-oxobenzenepropanoateHCID 2063901—
SolventEthanolHCID 702—
Product(Z)-Methyl 3-(2,4-dimethoxyphenyl)-3-((2-ethoxy-2-oxoethyl)amino)acrylateHCID 8668469569.2%

Reaction Conditions

Temperature100 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08835449B2
Source datasetuspto-grants-2014_09
ORD IDord-9921a0d60d1748beb999e57d661a0712
Source noteuspto-grants-2014_09