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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1243318Generated: October 26, 2026

Diethyl Oxalate → Ethyl 2-methoxybenzoylformate

https://huagongshe.com/reaction/1243318

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl OxalateHCID 7268—
Reactant2-BromoanisoleHCID 11358—
ReactantAmmonium ChlorideHCID 25517—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
SolventPentaneHCID 8003—
ProductEthyl 2-methoxybenzoylformateHCID 15579652—

Reaction Steps

A solution of 27 g of 1-bromo-2-methoxybenzene in 270 ml of ether is cooled to −70° C., under an argon atmosphere, 90 ml of a 1.6M solution of n-butyllithium in pentane are added dropwise and the mixture is then stirred for 45 minutes. 78 ml of diethyl oxalate are added quickly and the mixture is stirred while allowing the temperature to return to RT. After stirring for 1 hour at RT, saturated NH4Cl solution is added to the reaction mixture, the phases are separated by settling, the aqueous phase is extracted with ether, the combined organic phases are washed with water and with saturated NaCl solution and dried over Na2SO4, and the solvents are evaporated off under vacuum. The excess diethyl oxalate is removed by distillation under vacuum (b.p.=87° C. at 2000 Pa). The resulting product is chromatographed on silica gel, eluting with a DCM/hexane mixture (50/50; v/v) and then with DCM. The product obtained is purified by distillation under vacuum. 13 g of the expected product are obtained, b.p.=110° C. at 3 Pa.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07119086B2
Source datasetuspto-grants-2006_10
ORD IDord-4ff3f534616e481784f3cdd819481243
Source noteuspto-grants-2006_10