HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2105921Generated: October 28, 2026
4-Formylbenzoic acid → 4-(4-Methyl-1-piperazinylmethyl)benzoic acid
https://huagongshe.com/reaction/2105921
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Formylbenzoic acid | HCID 12088 | — |
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Platinum | HCID 23939 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-(4-Methyl-1-piperazinylmethyl)benzoic acid | HCID 4769782 | 70% |
Reaction Steps
A suspension of 4-formyl-benzoic acid (10.0 g, 67 mmol) in methanol (100 ml) is treated sequentially with 1-methylpiperazine (7.3 g, 73 mmol) and platinum (5%) on sulfided carbon (1 g). The resulting suspension is then heated at 80° C. and is subjected to a pressure of 5 bar of hydrogen for a period of 20 hrs until the hydrogen uptake is complete. The reaction mixture is cooled to room temperature and filtrated over a pad of Celite. Water (20 ml) is used to rinse the reactor and dissolve the fraction of 4-(4-methyl-piperazin-1-ylmethyl)-benzoic acid that crystallizes on the walls during the cooling of the reaction mixture. The resulting aqueous solution is filtrated over the pad of Celite employed previously. The combined filtrates are concentrated in vacuo and crystallized in EtOH/H2O 9:1 v/v to give 10.9 g (70%) of 4-(4-methyl-piperazin-1-ylmethyl)-benzoic acid as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07579467B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-fba3c05c0ad74217b5614678bdaa13cc |
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| Source note | uspto-grants-2009_08 |
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