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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 81834Generated: October 30, 2026

Potassium Carbonate → 1-[4-(4-Benzyl-piperazin-1-yl)-2-hydroxy-5-methoxy-phenyl]ethanone

https://huagongshe.com/reaction/81834

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-BenzylpiperazineHCID 75994—
Reactant1-(2-Benzyloxy-4-fluoro-5-methoxy-phenyl)-ethanoneHCID 59598748—
SolventDimethylformamideHCID 6228—
Product1-[4-(4-Benzyl-piperazin-1-yl)-2-hydroxy-5-methoxy-phenyl]ethanoneHCID 6705337985.3%

Reaction Conditions

Temperature135 °C

Reaction Steps

To a solution of 1-(2-Benzyloxy-4-fluoro-5-methoxy-phenyl)-ethanone (4.25 g, 15.5 mmol) in 3 mL DMF was added 1-benzyl-piperazine (5.4 mo, 30.9 mmol) and potassium carbonate (4.28 g, 30.9 mmol). The reaction mixture was heated under nitrogen to 130-140° C. for 18 hours. The reaction mixture was cooled to room temperature, poured into ice water, and extracted with EtOAc. The combined organic layers were washed with brine, dried (MgSO4), filtered, and evaporated under reduced pressure. The resulting residue was purified by flash chromatography on silica gel (hexanes:ethyl acetate 8.5:1.5) to yield 4.5 g (73%) of 1-[4-(4-Benzyl-piperazin-1-yl)-2-hydroxy-5-methoxy-phenyl]ethanone as a solid. MP=90-92° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846705B2
Source datasetuspto-grants-2014_09
ORD IDord-3b4d3c3c8f0945adb15e94446d2217d9
Source noteuspto-grants-2014_09