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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2046180Erstellt: 27. Oktober 2026

Diethyl Oxalate → 2,4-Dioxo-5-phenoxy-hexanoic acid ethyl ester

https://huagongshe.com/reaction/2046180

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethyl OxalateHCID 7268—
Edukt3-Phenoxy-2-butanoneHCID 2764474—
EduktSodiumHCID 5360545—
LösungsmittelEthanolHCID 702—
Produkt2,4-Dioxo-5-phenoxy-hexanoic acid ethyl esterHCID 6797460066,3%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

Sodium (82 mg, 3.55 mmol) was added to EtOH absolute (9.8 mL) at 0° C. The mixture was stirred at 0° C. until the sodium was completely dissolved. Then (rac)-3-phenoxy-butan-2-one (530 mg, 3.23 mmol) was added dropwise. The mixture was stirred at 0° C. for 10 minutes. Then diethyl oxalate (0.44 mL, 3.23 mmol) was added. Then the mixture was stirred at room temperature for 16 hours and the solvent evaporated in vacuo. The residue was diluted with water, the mixture acidified with a 1M solution of HCl and extracted with DCM. The organic layer was separated, dried (Na2SO4), filtered and the solvents evaporated in vacuo. The crude product was purified by open column chromatography (silica; DCM 100%) to yield (rac)-2,4-dioxo-5-phenoxy-hexanoic acid ethyl ester (566 mg, 58% yield) as an orange oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08592422B2
Quelldatensatzuspto-grants-2013_11
ORD IDord-69f8725c59d1439fa42b0bbbcabbe8db
Quellennotizuspto-grants-2013_11