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HRID 524045Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/524045

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethyl OxalateHCID 7268—
Edukt1-Bromo-3,5-dimethoxybenzeneHCID 639187—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktEthyl (3,5-dimethoxyphenyl)(oxo)acetateHCID 2472225671,4%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

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]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09340514B2
Quelldatensatzuspto-grants-2016_05
ORD IDord-d461a96576574a6ea8e603a13080f7ea
Quellennotizuspto-grants-2016_05