HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 248453Generated: October 26, 2026
Potassium Carbonate → (1,4-Dibenzylpiperazin-2-yl)methanol
https://huagongshe.com/reaction/248453
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Ethyl 1,4-dibenzylpiperazine-2-carboxylate | HCID 2736402 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (1,4-Dibenzylpiperazin-2-yl)methanol | HCID 10827800 | 103.2% |
Reaction Steps
A 3.06 g portion of lithium aluminum hydride in 130 ml of dry ether, with argon bubbling through the solution, was stirred at room temperature. A solution of 24.5 g of 1,4-bis(phenylmethyl)-2-piperazinecarboxylic acid, ethyl ester in 125 ml of dry ether was added, the mixture was heated at reflux for 5 hours and then cooled. A 40 ml portion of 40% aqueous potassium hydroxide followed by 80 ml of saturated aqueous potassium carbonate were added dropwise, under argon. The mixture was allowed to stand overnight, after stirring for one hour. The ether layer was removed and saved, then the remainder filtered. The filtrate was extracted several times with ether. The ether solutions were combined, dried, filtered and evaporated, giving 22.15 g of 1,4-bis(phenylmethyl)-2-piperazinemethanol as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05210193 |
|---|
| Source dataset | uspto-grants-1993_05 |
|---|
| ORD ID | ord-a652b59fbd174400b73fe4888044c90b |
|---|
| Source note | uspto-grants-1993_05 |
|---|