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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 44615Erstellt: 24. Oktober 2026

Ethyl benzoylformate → 1-[2-(Benzylthio)-8-oxo-5,6,7,8-tetrahydroquinazolin-7-yl]-2-phenylethane-1,2-dione

https://huagongshe.com/de/reaction/44615

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl benzoylformateHCID 15349—
EduktSodium hydrideHCID 24758—
Edukt2-(benzylthio)-6,7-dihydroquinazolin-8(5H)-oneHCID 57444113—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-[2-(Benzylthio)-8-oxo-5,6,7,8-tetrahydroquinazolin-7-yl]-2-phenylethane-1,2-dioneHCID 5744411468%

Reaktionsschritte

To a solution of 0.22 g (0.81 mmol) of 2-(benzylthio)-6,7-dihydroquinazolin-8(5H)-one in 5 mL of dry tetrahydrofuran cooled to −50° C., 0.10 g of sodium hydride 60% in mineral oil were added. The resulting suspension was maintained at the same temperature for 30 minutes and then 0.59 mL of ethyl α-oxobenzeneacetate (PhCOCOOEt) were added and the reaction mixture allowed to come to room temperature. After 16 hours the mixture was partitioned between water and ethyl acetate and the organic layer was dried over Na2SO4 and evaporated to dryness. The residue was purified by chromatography on a silica gel column (eluant hexane/ethyl acetate 7/3) giving 0.22 g (68% yield) of the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08541429B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-6cb9fd63185241d28ffc6683e788d26e
Quellennotizuspto-grants-2013_09