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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 498979Generated: October 29, 2026

1-Propanone, 1-(2-hydroxyphenyl)-3-phenyl- → HCID 11558573, compound

https://huagongshe.com/reaction/498979

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Propanone, 1-(2-hydroxyphenyl)-3-phenyl-HCID 77052—
ReactantNeohesperidinHCID 442439—
SolventHydrochloric AcidHCID 313—
ProductHCID 11558573HCID 11558573—

Reaction Conditions

Temperature80 °C

Reaction Steps

Neohesperidin is a glycoside of dihydrochalcone. A total weight of 100 mg of neohesperidin was suspended in 10 ml of 1N HCl and heated at 80° C. for 2 hours. The hydrolyzed product (10) was cooled down and extracted with ethyl acetate (3×10 ml). The ethyl acetate layers were combined, evaporated to remove ethyl acetate and dissolved in 1-propanol (5 ml). Sodium borohydride (25 mg) was added to the propanol solution and stirred at room temperature for 2 hours. After the completion of the reaction, the mixture was separated on a pre-packed C18 column eluting with a MeOH/H2O gradient to provide 1-(2,4,6-trihydroxyphenyl)-3-(3′-hydroxy-4′-methoxyphenyl)-1-propanol (11).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07767661B2
Source datasetuspto-grants-2010_08
ORD IDord-ec7c2000959f40388bf0ce38b2e60689
Source noteuspto-grants-2010_08