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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 37819Erstellt: 24. Oktober 2026

Diethyl Malonate → Diethyl tetrahydropyran-4,4-dicarboxylate

https://huagongshe.com/de/reaction/37819

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethyl MalonateHCID 7761—
EduktBis(2-chloroethyl) etherHCID 8115—
EduktSodium ethoxideHCID 2723922—
EduktSodiumHCID 5360545—
LösungsmittelEthanolHCID 702—
ProduktDiethyl tetrahydropyran-4,4-dicarboxylateHCID 23960644%

Reaktionsschritte

A solution of diethyl malonate (15.2 mL, 99.8 mmol) in ethanol (10 mL) was added dropwise to a solution of sodium ethoxide in ethanol [freshly prepared from sodium (2.3 g, 100 mmol) and ethanol (30 mL)] at ambient temperature and stirred for 10 min. Bis(2-chloroethyl)ether (12 mL, 102 mmol) was added dropwise then the mixture was heated at reflux overnight. It was then cooled to 10° C. before another portion of freshly-prepared sodium ethoxide in ethanol [prepared from sodium (2.3 g, 100 mmol) and ethanol (30 mL)] was added. The mixture was heated at reflux for 48 h then cooled, filtered to remove the precipitated sodium chloride then the filtrate was concentrated to dryness. Water was added to the residue which was then extracted with ether (3×25 mL). The combined ether layers were washed with water, brine and dried over anhydrous sodium sulfate. Concentration under reduced pressure yielded tetrahydropyran-4,4-dicarboxylic acid diethyl ester (10.1 g, 44%) as a mobile oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08524705B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-050e16850c5e47c4a229ebfd5571d562
Quellennotizuspto-grants-2013_09