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HRID 259654作成日:2026年10月26日

Ammonia → 1-Butylpiperazine

https://huagongshe.com/reaction/259654

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物Carbon DioxideHCID 280—
反応物Butylamine, N,N-bis(2-chloroethyl)-, hydrochlorideHCID 108674—
反応物Sodium ethoxideHCID 2723922—
溶媒EthanolHCID 702—
溶媒Diethyl EtherHCID 3283—
生成物1-ButylpiperazineHCID 424322—

反応条件

温度60 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04038391
出典データセットuspto-grants-1977_07
ORD IDord-80b0c1fd06c84340b43a5134a3d221e1
出典メモuspto-grants-1977_07