HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(3-Hydroxypropyl)piperazine-1-carbaldehyde → Piperazin-1-ylpropanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(3-Hydroxypropyl)piperazine-1-carbaldehyde | HCID 22490031 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Piperazin-1-ylpropanol | HCID 79207 | 63.1% |
Reaction Steps
A solution of 4-(3-hydroxypropyl)-1-piperazinecarboxaldehyde (4.45 g) in methanol (10 ml) and 4N aqueous hydrogen chloride (15 ml) was stirred at ambient temperature for 3 hours. The volatiles were removed under vacuum and the residue was partitioned between trichloromethane and aqueous sodium hydroxide (40%). The organic layer was separated, washed with brine, dried (MgSO4) and evaporated to give 3-(piperazin-1-yl)propan-1-ol (2.35 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06887874B2 |
| Source dataset | uspto-grants-2005_05 |
| ORD ID | ord-6660a21346944456979e281ff784a538 |
| Source note | uspto-grants-2005_05 |