首页> 外国专利> PREPARATION OF MINERAL ACID SALT OF ALPHAAHALOGENOOBETAA AMINOPROPIONITRILE

PREPARATION OF MINERAL ACID SALT OF ALPHAAHALOGENOOBETAA AMINOPROPIONITRILE

机译:阿尔法乙酰胆碱氨基丙酸矿物酸盐的制备。

摘要

PURPOSE:To obtain the titled compound in high purity in high yield useful as an intermediate for preparing an alpha-amino acid, by reacting an alpha,beta-dihalogenopropionitrile with ammonia in water and/or an organic solvent, followed by reacting the resulting product with a mineral acid. CONSTITUTION:1Mol alpha-beta-dihalogenopropionitrile is reacted with not less than 2mol ammonia in water and/or an organic solvent (e.g., methanol, ethanol, etc.) at -40-30 deg.C. Formed alpha-halogeno-beta-aminopropionitrile is extracted, and the extracted solution is reacted with a mineral acid (e.g., HCl, H2SO4,etc.) to give a mineral acid of an alpha-halogeno-beta-aminopropionitrile. The reaction may be carried out in air atmosphere, but the reaction in inert gas atmosphere, e.g., N2, etc. preferably prevents side reactions. Ammonia is used as 5-30wt% agueous ammonia or 2-25wt% ammonia in an organic solvent.
机译:目的:以高纯度获得高纯度标题化合物,用作制备α-氨基酸的中间体,方法是使α,β-二卤代丙腈与氨在水和/或有机溶剂中反应,然后使所得产物反应与无机酸。组成:1molα-β-二卤代丙腈在水和/或有机溶剂(例如甲醇,乙醇等)中于-40-30℃与不少于2摩尔的氨反应。提取形成的α-卤素-β-氨基丙腈,并将提取的溶液与无机酸(例如,HCl,H 2 SO 4等)反应,得到α-卤素-β-氨基丙腈的无机酸。该反应可以在空气气氛中进行,但是优选在惰性气体气氛如N 2等中进行,以防止副反应。氨用作有机溶剂中的5-30wt%的氨或2-25wt%的氨。

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