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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1180499Generated: November 1, 2026

Piperazine → Ammonia

https://huagongshe.com/reaction/1180499

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
Reactant1,2-DimethoxyethaneHCID 8071—
ReactantSodium HydroxideHCID 14798—
Reactant3-Chloro-5-ethoxypyridineHCID 11521128—
ReactantPotassium tert-butoxideHCID 23665647—
ProductAmmoniaHCID 222—
Product1-(5-Ethoxy-3-pyridyl)piperazine fumaric acid saltHCID 131724659—

Reaction Steps

A mixture of 3-chloro-5-ethoxypyridine (6.5 g, 45.8 mmol), piperazine (19.7 g, 229 mmol), potassium tert-butoxide (11.2 g, 91.6 mmol) and 1,2-dimethoxyethane (150 ml) was stirred at reflux for 1 hours. Aqueous sodium hydroxide (1 M, 100 ml) was added and the mixture was extracted two times with ethyl acetate (150 ml). Chromatography on silica gel with dichloromethane, methanol and conc. ammonia (89:10:1) gave the title compound. Yield 4.6 g, 48%. The corresponding salt was obtained by addition of a diethyl ether and methanol mixture (9:1) saturated with fumaric acid. Mp. 160.0-161.2° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07282494B2
Source datasetuspto-grants-2007_10
ORD IDord-02f2664e78974c5996de80c224fda553
Source noteuspto-grants-2007_10