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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1242066Erstellt: 26. Oktober 2026

Ethyl oxoacetate → Ethyl 4-oxo-3,4-dihydro-2H-pyran-2-carboxylate

https://huagongshe.com/reaction/1242066

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl oxoacetateHCID 70211—
Edukt1-Methoxy-3-trimethylsilyloxy-1,3-butadieneHCID 101051—
KatalysatorZincchlorideHCID 3007855—
LösungsmittelBenzeneHCID 241—
ProduktEthyl 4-oxo-3,4-dihydro-2H-pyran-2-carboxylateHCID 2249509775%

Reaktionsschritte

A solution of glyoxylic acid ethyl ester, polymer form (2.02 g, 8.9 mmol) and (3-methoxy-1-methylene-allyloxy)-trimethyl-silane (1.9 ml, 8.9 mmol, Danishefsky's diene) in benzene (12 ml) was placed under nitrogen. Zinc chloride (0.5N in tetrahydrofuran, 8.9 ml, 4.45 mmol) was added and the reaction stirred at ambient temperature for 72 h. The mixture was concentrated in vacuo, diluted with ethyl acetate (100 ml) and washed with 1 N hydrochloric acid (20 ml), saturated sodium bicarbonate (20 ml), and brine (20 ml). The organic layer was dried (Na2SO4), filtered, and the solvent evaporated in vacuo. The residue was purified by silica gel chromatography using a mixture of ethyl acetate/hexane (1:2) as eluant. Pure fractions were collected and the solvent evaporated in vacuo which afforded 1.2 g (75%) of 4-oxo-3,4-dihydro-2H-pyran-2-carboxylic acid ethyl ester as an oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07115624B1
Quelldatensatzuspto-grants-2006_10
ORD IDord-c3730e9cff94473b822c79093dd8dd0b
Quellennotizuspto-grants-2006_10