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Improvements in amino derivatives of n-alkyl substituted aspartic acids and their functional derivatives

机译:正烷基取代的天冬氨酸的氨基衍生物及其功能衍生物的改进

摘要

The invention comprises compounds of formula FORM:0757704/IV(a)/1 wherein X is an alkylene group which interposes 2 or 3 carbon atoms directly between the nitrogen atoms; R1 is hydrogen or a group H2N-X-; and R2 is hydrogen, sodium or an alkyl radical containing up to 18 carbon atoms. The compounds are prepared by reacting equimolar proportions of an alkylene polyamine H2N-X-NH-(X-NH)n-H (wherein n is 0 or 1) with a dialkyl (preferably diethyl) ester of maleic acid at a temperature below 50 DEG C., completing the reaction at 50-100 DEG C. and, if desired, saponifying the ester groups with caustic soda and recovering the corresponding sodium salts, from which the free acids may be obtained by acidification or ion exchange. The reaction is preferably conducted in a solvent such as benzene, toluene, dioxane or tertiary butamol. Amine starting materials are, for example, ethylene diamine, isopropylene diamine, trimethylene diamine, 1.3-diaminobutylene, 1.2-diaminobutylene, diethylene triamine, di-isopropylene triamine and di-(trimethylene) triamine. The examples describe the preparation of N-(2-aminoethyl)-, N-(2-aminoisopropyl)-, and N-(2-(2-aminoethyl)-aminoethyl)-aspartic acid, and the sodium salts and diethyl esters thereof. Specification 483,224, [Group IV], is referred to.
机译:本发明包括式的化合物,其中X是在氮原子之间直接插入2或3个碳原子的亚烷基。 R1是氢或H2N-X-基团; R2是氢,钠或含至多18个碳原子的烷基。通过在低于50℃的温度下使等摩尔比例的亚烷基多胺H 2 N-X-NH-(X-NH)n H(其中n为0或1)与马来酸的二烷基(优选二乙基)酯反应来制备化合物。例如,在50-100℃下完成反应,如果需要的话,用苛性钠将酯基皂化并回收相应的钠盐,通过酸化或离子交换可从中获得游离酸。该反应优选在溶剂如苯,甲苯,二恶烷或叔丁醇中进行。胺原料为例如乙二胺,异丙烯二胺,三亚甲基二胺,1.3-二氨基丁烯,1.2-二氨基丁烯,二亚乙基三胺,二异丙烯三胺和二-(三亚甲基)三胺。实施例描述了N-(2-氨基乙基)-,N-(2-氨基异丙基)-和N-(2-(2-氨基乙基)-氨基乙基)-天冬氨酸的制备及其钠盐和二乙基酯。 。参见规范483,224,[第IV组]。

著录项

  • 公开/公告号GB757704A

    专利类型

  • 公开/公告日1956-09-26

    原文格式PDF

  • 申请/专利权人 THE DOW CHEMICAL COMPANY;

    申请/专利号GB19530009240

  • 发明设计人

    申请日1953-04-02

  • 分类号C08L21/00;

  • 国家 GB

  • 入库时间 2022-08-23 22:47:07

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