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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 733181Erstellt: 26. Oktober 2026

2,2-Dimethyl-1,3-dioxane-4,6-dione → Ethyl 6-(benzyloxy)-3-oxohexanoate

https://huagongshe.com/reaction/733181

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2,2-Dimethyl-1,3-dioxane-4,6-dioneHCID 16249—
Edukt2-DimethylaminopyridineHCID 21885—
EduktIsopropenyl chloroformateHCID 93846—
EduktPotassium bisulfateHCID 516920—
Edukt4-(Benzyloxy)butanoic acidHCID 562201—
LösungsmittelDichloromethaneHCID 6344—
ProduktEthyl 6-(benzyloxy)-3-oxohexanoateHCID 10264779—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

4-Benzyloxybutyric acid (6.38 mL), Meldrum's acid (5.76 g) and dimethylaminopyridine (9.77 g) were dissolved in DCM (200 mL) and cooled to 0° C. A solution of isopropenyl chloroformate in dichloromethane (100 mL) was added dropwise and stirring at 0° C. continued for a further 2 h. Potassium hydrogen sulphate (200 mL of a 10% aqueous solution) was then added, the organic phase separated, dried over sodium sulphate, and evaporated under reduced pressure. The residue was dissolved in ethanol (200 mL) and heated at reflux overnight. Following cooling, the solvent was evaporated under reduced pressure and the resultant oil was purified by flash silica column chromatography. 6-Benzyloxy-3-oxo-hexanoic acid ethyl ester was isolated as an orange oil (8.53 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07589095B2
Quelldatensatzuspto-grants-2009_09
ORD IDord-89951e2fd3ce4e01a09824d7d1d6ead2
Quellennotizuspto-grants-2009_09