Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 442413Erstellt: 23. Oktober 2026

Carbon Dioxide → Phenylbenzylglyoxal

https://huagongshe.com/de/reaction/442413

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCarbon DioxideHCID 280—
EduktWaterHCID 962—
EduktChalcone epoxideHCID 92219—
EduktPotassium tert-butoxideHCID 23665647—
LösungsmittelEthanolHCID 702—
ProduktPhenylbenzylglyoxalHCID 1109623465%

Reaktionsschritte

To a boiling solution of 30 g 1,3-diphenyl-2,3-epoxy-1-propanone in 500 ml ethanol was rapidly added a hot solution of 30 g potassium t-butoxide in 500 ml ethanol. The mixture was kept boiling on a steambath for 2 minutes. It was then diluted with 3 l. water. The aqueous solution was saturated with carbon dioxide by the addition of small pieces of dry ice. The resulting emulsion was extracted with ether. The ether extracts were diluted with benzene, dried over sodium sulfate and evaporated under reduced pressure. The remaining dark oil was distilled in high vacuum to afford 19.5 g 1,3-diphenyl-1,2-propanedione; b.p. 136°-138°/0.1 mm.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04045487
Quelldatensatzuspto-grants-1977_08
ORD IDord-972728a6b5bd4f92b2f0a83fcfe80e4f
Quellennotizuspto-grants-1977_08