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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2253274Generated: November 1, 2026

Hydrochloric Acid → 2-(4-{4-[3-(3-Cyclohexylureido)-3-Oxopropyl]-Phenoxy}-Phenyl)-3-(3,5-Dimethoxyphenyl)-Acrylic Acid

https://huagongshe.com/reaction/2253274

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTrifluoroacetic acidHCID 6422—
ReactantCyclohexylureaHCID 69684—
ReactantHCID 69131096HCID 69131096—
SolventEthanolHCID 702—
SolventSodium ethoxideHCID 2723922—
Product2-(4-{4-[3-(3-Cyclohexylureido)-3-Oxopropyl]-Phenoxy}-Phenyl)-3-(3,5-Dimethoxyphenyl)-Acrylic AcidHCID 69130265—

Reaction Conditions

Temperature75 °C

Reaction Steps

Cyclohexylurea (1.3 g, 9 mmol) was dissolved in sodium ethoxide in ethanol (21% w/w, 3 mL) at 75° C. To this solution 5 was added (0.5 g, 1.1 mmol) in one lot. The resulting mixture was stirred at 75° C. for 5 min, then cooled quickly to 40-50° C. TFA (0.5 mL) was added and then 5% aqueous HCl (1N, 0.6 mL). After stirring at room temperature for 1 hr, the mixture was left overnight at 4° C. The solid separated was filtered and refluxed in ethyl acetate (4 mL) for 20 min. The mixture was allowed to cool to room temperature, filtered and the crude product was purified by silica gel chromatography using hexane-ethyl acetate (1:1). Yield: 0.27 g, 45%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07323496B2
Source datasetuspto-grants-2008_01
ORD IDord-5b6832600898468d80bc84d955293681
Source noteuspto-grants-2008_01