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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1893695Generated: October 31, 2026

Ethyl Acetate → 1-[2-Amino-3-chloro-4-(2,2-dimethoxy-ethoxy)-phenyl]-ethanone

https://huagongshe.com/reaction/1893695

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantCesium carbonateHCID 10796—
Reactant2-Bromo-1,1-dimethoxyethaneHCID 81672—
Reactant1-(2-Amino-3-chloro-4-hydroxy-phenyl)-ethanoneHCID 57445195—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product1-[2-Amino-3-chloro-4-(2,2-dimethoxy-ethoxy)-phenyl]-ethanoneHCID 5744519667%

Reaction Conditions

Temperature65 °C

Reaction Steps

1-(2-Amino-3-chloro-4-hydroxyphenyl)ethanone (40 g, 215 mmol) was dissolved in DMF (360 ml). Cesium carbonate (140 g, 430 mmol) was added, followed by bromoacetaldehyde dimethyl acetal (54.5 g, 323 mmol). The mixture was then vigorously stirred at 65° C. for 24 h. Upon cooling to room temperature, EtOAc (1 L) and H2O (1 L) were added to the mixture. The organic layer was extracted with EtOAc (1×400 ml). The combined organic layer was washed with aqueous 3% LiCl solution (2×1 L), brine, dried (Na2SO4) and concentrated in vacuo. The residue was purified by silica gel chromatography to give 1-[2-amino-3-chloro-4-(2,2-dimethoxyethoxy)phenyl]-ethanone as a white solid (39 g, 67% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08513186B2
Source datasetuspto-grants-2013_08
ORD IDord-ebdec2ca51ec42b696e215453183bbf0
Source noteuspto-grants-2013_08