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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 524045Generated: October 25, 2026

Diethyl Oxalate → Ethyl (3,5-dimethoxyphenyl)(oxo)acetate

https://huagongshe.com/reaction/524045

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl OxalateHCID 7268—
Reactant1-Bromo-3,5-dimethoxybenzeneHCID 639187—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductEthyl (3,5-dimethoxyphenyl)(oxo)acetateHCID 2472225671.4%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 1-bromo-3,5-dimethoxybenzene (2.17 g, 10 mmol) in THF (15 mL) was dropwise added n-butyl lithium (8 mL, 2.5 mol/L in hexane, 20 mmol) at −78° C. After stirring for 50 mins at −78° C. a solution of diethyl oxalate (4 g, 27 mmol) in THE (10 mL) was added. The mixture was stirred at −78° C. for another 4 h, then quenched with saturated ammonium chloride and extracted with ethyl acetate (50 mL*3). The organic layers were combined, washed by brine, dried over sodium sulfate, filtered and concentrated. The residue was purified by chromatography on silica gel to give the title compound (1.7 g, 71%). MS (ES+) C12H14O5 requires: 238. found: 239 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09340514B2
Source datasetuspto-grants-2016_05
ORD IDord-d461a96576574a6ea8e603a13080f7ea
Source noteuspto-grants-2016_05