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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2180140Generated: October 30, 2026

4-(3-Hydroxypropyl)piperazine-1-carbaldehyde → Piperazin-1-ylpropanol

https://huagongshe.com/reaction/2180140

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(3-Hydroxypropyl)piperazine-1-carbaldehydeHCID 22490031—
SolventHydrochloric AcidHCID 313—
SolventMethanolHCID 887—
ProductPiperazin-1-ylpropanolHCID 7920763.1%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06887874B2
Source datasetuspto-grants-2005_05
ORD IDord-6660a21346944456979e281ff784a538
Source noteuspto-grants-2005_05