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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 259654Generated: October 25, 2026

Ammonia → 1-Butylpiperazine

https://huagongshe.com/reaction/259654

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantCarbon DioxideHCID 280—
ReactantButylamine, N,N-bis(2-chloroethyl)-, hydrochlorideHCID 108674—
ReactantSodium ethoxideHCID 2723922—
SolventEthanolHCID 702—
SolventDiethyl EtherHCID 3283—
Product1-ButylpiperazineHCID 424322—

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution (447 cc.) of sodium ethoxide in ethanol of concentration 1.34 moles per liter, followed by a solution (1,305 cc.) of ammonia in ethanol of concentration 4.6 moles per liter, are added to a suspension of N,N-bis(2-chloroethyl)butylamine hydrochloride (140.7 g.) in ethanol (750 cc.). The reaction mixture is then heated at a temperature of about 60° C. for 1 hour, whilst keeping the ammonia refluxing by means of a condensor containing solid carbon dioxide. The ammonia is then allowed to dissipate, and the reaction mixture is cooled to a temperature of about 20° C. under a stream of nitrogen. A solution (894 cc.) of sodium ethoxide in ethanol of concentration 1.34 moles per liter is then added. The sodium chloride which precipitates is filtered off and then washed with ethanol (150 cc.). The filtrate is concentrated to dryness under reduced pressure and the residue obtained is taken up in diethyl ether (300 cc.). The insoluble product is filtered off and washed with diethyl ether (60 cc.). The filtrate is concentrated to dryness and then distilled under reduced pressure. 1-t.-Butylpiperazine (8.8 g.), which boils at 85°-86° C. under a pressure of 28 mm. Hg, is thus obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04038391
Source datasetuspto-grants-1977_07
ORD IDord-80b0c1fd06c84340b43a5134a3d221e1
Source noteuspto-grants-1977_07