HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 1,4-dibenzylpiperazine-2-carboxylate → (1,4-Dibenzylpiperazin-2-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 1,4-dibenzylpiperazine-2-carboxylate | HCID 2736402 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (1,4-Dibenzylpiperazin-2-yl)methanol | HCID 10827800 | 87.9% |
Reaction Steps
Lithium aluminium hydride (1 M solution in tetrahydrofuran, 32 ml, 32 mmol) at 0° C. was treated dropwise with a solution of 1,4-dibenzyl-piperazine-2-carboxylic acid ethyl ester (10 g, 32.1 mmol) in tetrahydrofuran (30 ml) and stirred for 16 hours. The mixture was quenched by slow addition of sodium hydroxide solution (4 M, 150 ml), followed by dichloromethane (200 ml). The organic phase was separated, dried with sodium sulfate and evaporated to afford 1,4-dibenzyl-2-(hydroxymethyl)piperazine (8.36 g) as an orange oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07304064B2 |
| Source dataset | uspto-grants-2007_12 |
| ORD ID | ord-c2a3eb0f67154f1188ea22c13bbda9e7 |
| Source note | uspto-grants-2007_12 |