YAKUGAKU ZASSHI
Online ISSN : 1347-5231
Print ISSN : 0031-6903
ISSN-L : 0031-6903
ピペラジン及びN-アルキルピペラジンの合成 (第1報)
石黒 武雄北村 英一松村 正毅
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ジャーナル フリー

1953 年 73 巻 10 号 p. 1110-1114

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Heating of diethanolamine hydrochloride at 200-230° results in the formation of morpholine alone, but the same at 230-240° gives morpholine and piperazine. The product from the heating at 250-260° is chiefly piperazine and only a small amount of morpholine is formed. N-Alkyldiethanolamine hydrochloride also forms N-alkylmorpholine and N-alkylpiperazine by heating. Both morpholine and N-alkylmorpholine undergo partial decomposition when heated at a high temperature to form piperazine and N-alkylpiperazine, respectively. By heating a mixture of diethanolamine hydrochloride and monoalkylamine hydrochloride at 250-260° for 3-4 hours, N-monoalkylpiperazine is obtained in 20-30% yield of the theoretical amount. Similar heating of the mixture of the hydrochloride of diethanolamine and dialkylamine also yields N-monoalkylpiperazine. Heating of a mixture of the hydrochloride of diethanolamine or N-alkyldiethanol-amine and ammonium chloride also results in the formation of the corresponding piperazine or N-monoalkylpiperazine in 20-25% yield of the theoretical amount. Morpholine, piperazine, and N-alkylmorpholine are formed as by-products in these reactions.

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© by the PHARMACEUTICAL SOCIETY OF JAPAN
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