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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Benzylpiperazine | HCID 75994 | — |
| Reactant | 1-(2-Benzyloxy-4-fluoro-5-methoxy-phenyl)-ethanone | HCID 59598748 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-[4-(4-Benzyl-piperazin-1-yl)-2-hydroxy-5-methoxy-phenyl]ethanone | HCID 67053379 | 85.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08846705B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-3b4d3c3c8f0945adb15e94446d2217d9 |
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| Source note | uspto-grants-2014_09 |
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