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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1868533Generated: October 31, 2026

Hydrochloric Acid → 4H-1-Benzopyran-4-one, 2,2'-(1,4-phenylene)bis(3-hydroxy-

https://huagongshe.com/reaction/1868533

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHydrogen PeroxideHCID 784—
ReactantTerephthalaldehydeHCID 12173—
ReactantSodium HydroxideHCID 14798—
Reactantalpha-HydroxyacetophenoneHCID 68490—
SolventMethanolHCID 887—
Product4H-1-Benzopyran-4-one, 2,2'-(1,4-phenylene)bis(3-hydroxy-HCID 265727—

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 ml), Terephthalaldehyde (0.98 g) and 2-hydroxy acetophenone (2.04 g). The reaction mixture was cooled to 10-15° C. and sodium hydroxide (3 g) was added slowly and the reaction was stirred at room temperature (˜25° C.) for 24 hrs. Then methanol (200 ml) was added to the reaction and the reaction mixture was cooled below 15° C. and sodium hydroxide (3 g) and hydrogen peroxide (9 ml) were added to the reaction mixture and the reaction mixture was stirred for 6-8 hrs at room temperature. After this the reaction mixture was cooled to 10° C., neutralized using hydrochloric acid and the solid product that precipitated was filtered. The solid was washed with water till the filtrate is free of acid. The solid product was dried in oven at 70° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07635778B2
Source datasetuspto-grants-2009_12
ORD IDord-d016301f2514429b8ac655eae3dca658
Source noteuspto-grants-2009_12