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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2405845Generated: November 2, 2026

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

https://huagongshe.com/reaction/2405845

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 numberUS08809267B2
Source datasetuspto-grants-2014_08
ORD IDord-3d6471831bbe476c9e58b9a7f244e20e
Source noteuspto-grants-2014_08