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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 230894Generated: October 27, 2026

Water → 2'-Carboxymethoxy-6'-hydroxy-3-(2-hydroxyethoxy)dihydrochalcone

https://huagongshe.com/reaction/230894

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium HydroxideHCID 14797—
ReactantBenzaldehyde, 3-(2-hydroxyethoxy)-HCID 6453965—
Reactant6'-Hydroxy-2'-(methoxycarbonylmethoxy)acetophenoneHCID 10537084—
CatalystHCID 178418390HCID 178418390—
SolventEthanolHCID 702—
Product2'-Carboxymethoxy-6'-hydroxy-3-(2-hydroxyethoxy)dihydrochalconeHCID 6713580799.7%

Reaction Steps

To a suspension of 6′-hydroxy-2′-(methoxycarbonylmethoxy)acetophenone (1 g) and 3-(2-hydroxyethoxy)benzaldehyde (0.74 g) in ethanol (12 mL) were added water (3 mL) and potassium hydroxide (3 g), and the mixture was stirred at room temperature overnight. To the reaction mixture was added 10% palladium-carbon powder (0.2 g), and the mixture was stirred at room temperature under a hydrogen atmosphere for 8 hours. The insoluble material was removed by filtration, and the solvent of the filtrate was removed under reduced pressure. The residue was dissolved in water, and the solution was washed with diethyl ether. The aqueous layer was acidified by addition of concentrated hydrochloric acid, and the resulting mixture was extracted with ethyl acetate twice. The extract was washed with brine and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure. The residue was treated with diethyl ether, and the precipitated crystals were collected by filtration. The crystals were dried under reduced pressure to give the title compound (1.6 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07566699B2
Source datasetuspto-grants-2009_07
ORD IDord-78b6c384e39f49b6bba136e99252fe37
Source noteuspto-grants-2009_07