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HRID 259654생성일: 2026년 10월 24일

Ammonia → 1-Butylpiperazine

https://huagongshe.com/ko/reaction/259654

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물Carbon DioxideHCID 280—
반응물Butylamine, N,N-bis(2-chloroethyl)-, hydrochlorideHCID 108674—
반응물Sodium ethoxideHCID 2723922—
용매EthanolHCID 702—
용매Diethyl EtherHCID 3283—
생성물1-ButylpiperazineHCID 424322—

반응 조건

온도60 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04038391
출처 데이터셋uspto-grants-1977_07
ORD IDord-80b0c1fd06c84340b43a5134a3d221e1
출처 메모uspto-grants-1977_07