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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1160124Generated: October 28, 2026

4-Formylbenzoic acid → 4-(4-Methyl-1-piperazinylmethyl)benzoic acid

https://huagongshe.com/reaction/1160124

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Formylbenzoic acidHCID 12088—
Reactant1-MethylpiperazineHCID 53167—
ReactantHCID 178418361HCID 178418361—
CatalystPlatinumHCID 23939—
SolventMethanolHCID 887—
Product4-(4-Methyl-1-piperazinylmethyl)benzoic acidHCID 476978270%

Reaction Conditions

Temperature80 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07816359B2
Source datasetuspto-grants-2010_10
ORD IDord-f40be2fee7c84383974ccecb697174ac
Source noteuspto-grants-2010_10