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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2232397Generated: October 30, 2026

Piperazine → 1-(2-Methylpyridin-4-yl)piperazine

https://huagongshe.com/reaction/2232397

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
Reactant1-PentanolHCID 6276—
ReactantSodium BicarbonateHCID 516892—
Reactant4-Chloro-2-methylpyridine nitrateHCID 67865686—
SolventWaterHCID 962—
Product1-(2-Methylpyridin-4-yl)piperazineHCID 1676237760.2%

Reaction Steps

A mixture of 4-chloro-2-methylpyridine nitrate (5.00 g), piperazine (9.00 g), anhydrous sodium bicarbonate (6.60 g) and amyl alcohol (60 ml) was heated under reflux for 18 hours. The mixture was cooled and water was added to dissolve inorganic material. The organic layer was washed four times with brine and all the aqueous extracts were combined and extracted with ethyl acetate. The organic layers were combined, dried over sodium sulphate and evaporated. The residue was crystallised from ethyl acetate/hexane to give 1-(2-methylpyrid-4-yl)piperazine (2.80 g), m.p. 93°-94° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04788196
Source datasetuspto-grants-1988_11
ORD IDord-bacd9710458a40828c4143183fc73e44
Source noteuspto-grants-1988_11