HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 228109Generated: October 25, 2026
Lithium Hydroxide → 2-(4-Benzylpiperazin-1-yl)benzoic acid
https://huagongshe.com/reaction/228109
Participants
| Role | Name | HCID | Charge |
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| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | Methyl 2-[4-benzylpiperazinyl]benzoate | HCID 21935101 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(4-Benzylpiperazin-1-yl)benzoic acid | HCID 21935193 | 93.5% |
Reaction Steps
To a 150 mL round-bottomed flask equipped with magnetic stirring was added methyl 2-[4-benzylpiperazinyl]benzoate (Preparation XIII) (2.3 g, 7.4 mmol) in THF (60 mL). A soln of LiOH (Aldrich) (940 mg, 22 mmol) in H2O (20 mL), was added and the reaction mixture was heated at 60° C. for 12 h. After cooling to RT, the reaction mixture was concentrated in vacuo and diluted with EtOAc (100 mL). A 10% soln of citric acid (25 mL) was added, the organic layer was separated and the aqueous layer was extracted with EtOAc (2×25 mL). The organic layers were combined, washed with H2O, satd NaCl, dried over Na2SO4, filtered and concentrated in vacuo to afford 2-[4-benzylpiperazinyl]benzoic acid as a white solid (2.05 g). MS (ESI, pos. ion) m/z: 297 (M+H). Calc'd for C18H20N2O2: 296.15: 296.15.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07560460B2 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-618bbebec5f14112b114cf8e7b7006b4 |
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| Source note | uspto-grants-2009_07 |
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