Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 323184Generated: October 31, 2026

Ethyl bromoacetate → 3-Cyano-3-(3,4-dimethoxyphenyl)pentanedioic diethyl ester

https://huagongshe.com/reaction/323184

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantTetrahydrofuranHCID 8028—
Reactant3,4-DimethoxybenzeneacetonitrileHCID 66727—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
ReactantEthyl acetate hexaneHCID 21226206—
Product3-Cyano-3-(3,4-dimethoxyphenyl)pentanedioic diethyl esterHCID 15392019—

Reaction Conditions

Temperature10 °C

Reaction Steps

Combine 3,4-dimethoxyphenylacetonitrile (20 g, 113 mmol) and anhydrous tetrahydrofuran (100 mL). Cool in a dry-ice/acetone bath. Add dropwise a solution of sodium bis(trimethylsilyl)amide (226 mL, 1 M in THF, 226 mmol). When the addition is complete warm the reaction mixture to 10° C. and allow to stir for 15 minutes. Cool in a dry-ice/acetone bath, add dropwise ethyl bromoacetate (37.7 g, 226 mmol). When the addition of ethyl bromoacetate is complete, warm the reaction mixture to ambient temperature. After 18 hours, partition the reaction mixture between diethyl ether and water. Extract the organic layer with water and saturated aqueous solution of ammonium chloride. Separate the organic layer, dry over MgSO4, filter, and concentrate in vacuo to obtain a residue. Chromatograph the residue on silica gel eluting with 33% ethyl acetate/hexane. Remove residual solvent in vacuo at 82° C. to give the title compound: Rf=0.37 (silica gel, 33% ethyl acetate/hexane). Elemental Analysis calculated for C18H23NO6: C 61.88; H 6.64; N 4.01; Found: C 61.79; H 6.62; N 3.91.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06211199B1
Source datasetuspto-grants-2001_04
ORD IDord-5d243f3bdae24f85aa282a7f44667c9e
Source noteuspto-grants-2001_04