HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1242723Generated: October 25, 2026
Potassium Carbonate → Methyl 2-[4-benzylpiperazinyl]benzoate
https://huagongshe.com/reaction/1242723
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Benzoic acid, 2-fluoro-, methyl ester | HCID 67854 | — |
| Reactant | 1-Benzylpiperazine | HCID 75994 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Methyl 2-[4-benzylpiperazinyl]benzoate | HCID 21935101 | 58% |
Reaction Steps
To a 250 mL pressure bottle equipped with magnetic stirring was added methyl 2-fluorobenzoate (Lancaster Synthesis Inc.) (3.0 g, 20 mmol), 1-benzylpiperazine (Aldrich) (3.8 g, 22 mmol) and K2CO3 (3.0 g, 22 mmol) in DMF (100 mL) The mixture was heated at 150° C. for 12 h. After cooling to RT the reaction was diluted with EtOAc (100 mL) and H2O was added. The organic layer was separated and washed with H2O, brine, dried over Na2SO4, filtered and concentrated in vacuo to afford a brown oil. The crude material was purified by column chromatography (4:1 hexanes-EtOAc) to give the title compound as a white foam (3.6 g). MS (ESI, pos. ion) m/z: 311 (M+H). Calc'd for C19H22N2O2: 310.17.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07115607B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-84716c873d22431c8dbabc8eb4e5cfdb |
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| Source note | uspto-grants-2006_10 |
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