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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1833244Generated: October 31, 2026

Ethanol → Ethyl cyano(3,4-dimethoxyphenyl)acetate

https://huagongshe.com/reaction/1833244

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantDiethyl CarbonateHCID 7766—
Reactant3,4-DimethoxybenzeneacetonitrileHCID 66727—
ReactantSodiumHCID 5360545—
SolventTolueneHCID 1140—
SolventEthyl acetate hexaneHCID 21226206—
ProductEthyl cyano(3,4-dimethoxyphenyl)acetateHCID 12814070440.1%

Reaction Conditions

Temperature85 °C

Reaction Steps

Ethanol (13 mL, 225) was added to a suspension of sodium (3.6 g, 157 mmol) in toluene (125 mL) with stirring at 85° C. The reaction mixture turned to a slightly turbid white mixture. 3,4-Dimethoxy phenylacetonitrile (26.6 g, 150 mmol) was added to the reaction mixture at one time and the mixture was stirred at 85° C. for 30 minutes. Diethyl carbonate (20 mL, 16.5 mmol) was added to the mixture. The mixture was heated at 110° C. for 5 hrs. The solvent was evaporated and ice (250 g) was added. The mixture was neutralized to pH=7 by addition of acetic acid (20 mL). The aqueous phase was extracted with ethyl acetate (3×20 mL). The combined extracts were washed with saturated aqueous sodium chloride solution (50 mL), dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo. Flash chromatography (Merck Silica gel 60, 70–230 mesh, 40% ethyl acetate/hexane) afforded cyano-(3,4-dimethoxy-phenyl)-acetic acid ethyl ester (18.1 g, 49% yield) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07067529B2
Source datasetuspto-grants-2006_06
ORD IDord-327062fdc8414dc898335ddb62b5af22
Source noteuspto-grants-2006_06