HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1505608Generated: October 30, 2026
Potassium Carbonate → 4-(4-Acetylpiperazin-1-yl)benzaldehyde
https://huagongshe.com/reaction/1505608
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Fluorobenzaldehyde | HCID 68023 | — |
| Reactant | 1-Acetylpiperazine | HCID 83795 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-(4-Acetylpiperazin-1-yl)benzaldehyde | HCID 2052146 | 64% |
Reaction Steps
To a solution of 4-fluorobenzaldehyde (5 g, 40.2 mmol) in N,N-dimethylformamide (130 mL) was added potassium carbonate (8.35 g, 60.4 mmol) and 1-piperazin-1-ylethanone (10.3 g, 80.5 mmol) and the reaction was stirred at 130° C. for 16 hours. The reaction was then cooled to ambient temperature, diluted with EtOAc and washed with water (×2) and brine. The organic layer was then dried with MgSO4, concentrated and purified by silica gel column chromatography (0-10% methanol in dichloromethane) to give 4-(4-acetylpiperazin-1-yl)benzaldehyde (5.96 g, 64% yield). LCMS (m/z) ES+ 233 [M+1]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09216988B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-41557fbca4704720bb353daa05f19906 |
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| Source note | uspto-grants-2015_12 |
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