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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1925665Erstellt: 23. Oktober 2026

Benzaldehyde → Flavonol

https://huagongshe.com/de/reaction/1925665

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzaldehydeHCID 240—
EduktHydrochloric AcidHCID 313—
EduktHydrogen PeroxideHCID 784—
EduktSodium HydroxideHCID 14798—
Eduktalpha-HydroxyacetophenoneHCID 68490—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
ProduktFlavonolHCID 11349—

Reaktionsbedingungen

Temperatur12.5 °C

Reaktionsschritte

To a three necked round bottomed flask, equipped with reflux condenser, calcium chloride guard tube and nitrogen inlet and magnetic stirrer, was charged methanol (200 milliliters (ml)), benzaldehyde (10.6 grams (g)) and 2-hydroxy acetophenone (13.6 g). The mixture was cooled to 10-15° C. and sodium hydroxide (15 g in 40 milliliters (ml) water) was slowly added. The reaction mixture was stirred at room temperature (˜25° C.) for 24 hours. Then methanol was added to the reaction mixture and the mixture was cooled to below 15° C. To this cooled mixture sodium hydroxide (15 g in 40 ml water) and hydrogen peroxide (56 ml) were added and the reaction mixture was stirred for 6 to 8 hrs at room temperature. After this the reaction mixture was cooled to 10° C., neutralized using hydrochloric acid and the solid product that precipitated out was filtered. The solid was washed with water till the filtrate was free of acid. The solid product was dried in an oven at 70° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08178702B2
Quelldatensatzuspto-grants-2012_05
ORD IDord-436f4acb9d1c4477ae4801520d2e697c
Quellennotizuspto-grants-2012_05