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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 31348Generated: October 25, 2026

Hydrochloric Acid → Ethyl (2,6-dimethoxyphenyl)(oxo)acetate

https://huagongshe.com/reaction/31348

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl OxalateHCID 7268—
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
Reactant1,3-DimethoxybenzeneHCID 9025—
ReactantButyllithiumHCID 178418339—
SolventHexaneHCID 8058—
ProductEthyl (2,6-dimethoxyphenyl)(oxo)acetateHCID 22560922—

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 28 g of 1,3-dimethoxybenzene and 24.3 g of TMEDA in 400 ml of hexane is cooled to a temperature below 10° C., 132 ml of a 1.6 M solution of n-butyllithium in hexane are added dropwise and the mixture is left stirring for 30 minutes. The reaction mixture is cooled to 0° C., 140 ml of diethyl oxalate are added over 15 minutes and the mixture is left stirring for 1 hour at RT. The reaction mixture is poured into a mixture of concentrated HCl solution and ice and is extracted with EtOAc, the organic phase is washed with water and dried over Na2SO4, and the solvent is evaporated off under vacuum. The excess diethyl oxalate is removed by distillation under vacuum (b.p.=90° C. at 2 400 Pa). The resulting crude product is chromatographed on silica gel, eluting with heptane and then with DCM. 34.5 g of the expected product are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07425566B2
Source datasetuspto-grants-2008_09
ORD IDord-c4237ed6a1d84c4ca70925d0e30a025d
Source noteuspto-grants-2008_09