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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 442791Generated: October 25, 2026

Monoethyl malonate → Ethyl 3-methoxy-4-methoxycarbonylbenzoylacetate

https://huagongshe.com/reaction/442791

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMonoethyl malonateHCID 70615—
Reactant3-Methoxy-4-methoxycarbonylbenzoyl chlorideHCID 15161968—
ReactantButyllithiumHCID 178418339—
SolventHydrochloric AcidHCID 313—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductEthyl 3-methoxy-4-methoxycarbonylbenzoylacetateHCID 53689794—

Reaction Steps

To a solution of ethyl hydrogen malonate (4.38 g, 33.2 mmol) in dry tetrahydrofuran (100 ml) cooled under an atmosphere of nitrogen to -60° C. with efficient stirring was added a solution of n-butyllithium in hexane (2.5M, 26.5 ml) rapidly dropwise, allowing the temperature to rise to -10° C. during the addition. After stirring the resulting suspension for 15 min at -10° C. it was recooled to -70° C. and a solution of 3-methoxy-4-methoxycarbonylbenzoyl chloride (4.46 g, 19.5 mmol) in dry tetrahydrofuran (30 ml) added dropwise. After addition, the reaction mixture was allowed to warm to room temperature and after 1 h diluted with cold aqueous hydrochloric acid (2M, 35 ml) and ice. The mixture was extracted with diethyl ether (200 ml) and the extract washed twice with a saturated solution of sodium bicarbonate, water and a saturated solution of sodium chloride. The organic layer was dried over magnesium sulphate, filtered and evaporated. The residue was purified on flash silica eluting with dichloromethane to give ethyl 3-methoxy-4-methoxycarbonylbenzoylacetate as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05891899
Source datasetuspto-grants-1999_04
ORD IDord-3f77f296a0f74d6180ea08ed8755bd36
Source noteuspto-grants-1999_04