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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 31354Erstellt: 24. Oktober 2026

Diethyl Oxalate → Ethyl 2-methoxybenzoylformate

https://huagongshe.com/de/reaction/31354

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethyl OxalateHCID 7268—
Edukt2-BromoanisoleHCID 11358—
EduktAmmonium ChlorideHCID 25517—
EduktButyllithiumHCID 178418339—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelPentaneHCID 8003—
ProduktEthyl 2-methoxybenzoylformateHCID 15579652—

Reaktionsschritte

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 1.6 M solution of n-butyl-lithium in pentane are added dropwise and the mixture is then left stirring for 45 minutes. 78 ml of diethyl oxalate are added rapidly and the mixture is left stirring, while allowing the temperature to return to RT. After stirring for 1 hour at RT, saturated NH4Cl solution is added to the mixture, the phases are separated after settling has taken place, the aqueous phase is extracted with ether, the combined organic phases are washed with water and then 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 2 000 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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07425566B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-e1496e4568d7464da8f731298c452447
Quellennotizuspto-grants-2008_09