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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1868532Generated: October 26, 2026

Benzaldehyde → Flavonol

https://huagongshe.com/reaction/1868532

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantHydrochloric AcidHCID 313—
ReactantHydrogen PeroxideHCID 784—
ReactantSodium HydroxideHCID 14798—
Reactantalpha-HydroxyacetophenoneHCID 68490—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductFlavonolHCID 11349—

Reaction Conditions

Temperature12.5 °C

Reaction Steps

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 mililiters (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 mixuture 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07635778B2
Source datasetuspto-grants-2009_12
ORD IDord-c0d3f1d8035d487590948812133820a3
Source noteuspto-grants-2009_12