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    • 5. 发明专利
    • Preparation of cystine and cysteine
    • CYSTINE和CYSTEINE的制备
    • JPS59167561A
    • 1984-09-21
    • JP4061183
    • 1983-03-14
    • Showa Denko Kk
    • KAMETAKA TOKUOSOYA SUMIOHIROMOTO KAZUHIKOISHIOKA RIYOUJI
    • C07C319/02C07C67/00C07C313/00C07C319/24C07C323/58
    • PURPOSE: To obtain the titled amino acid useful as a drug, feed, etc. in high yield, by reacting β-chloroalanine with an alkali metal or ammonium polysulfide in an aqueous medium.
      CONSTITUTION: β-Chloroalanine is reacted with an alkali metal or ammonium polysulfide (e.g., sodium sulfide) in an aqueous medium or organic solvent (e.g., n-hexane) to give cystine, which is reduced to give cysteine. The reaction is usually carried out in a molar ratio of β-chloroalanine to the polysulfide of the alkali metal, etc. to (1: 1.0W about 5.0), the reaction temperature is preferably 5°CW the boiling point of the reaction solution and 20W100°C. β-Chloroalanine is almost completely converted into cystine and cysteine (or its S-alkali metal or ammonium salt), and cysteine and its salt is easily converted into cystine by acid treatment or oxidation reaction.
      COPYRIGHT: (C)1984,JPO&Japio
    • 目的:通过使β-氯丙氨酸与水性介质中的碱金属或多硫化铵反应,以高产率获得用作药物,饲料等的标题氨基酸。 构成:将β-氯丙氨酸与水性介质或有机溶剂(例如正己烷)中的碱金属或多硫化铵(例如硫化钠)反应,得到胱氨酸,将其还原得到半胱氨酸。 反应通常以β-氯丙氨酸与碱金属等的多硫化物的摩尔比等进行到(1:1.0-约5.0),反应温度优选为5℃ - 反应的沸点 溶液和20-100℃。 β-氯丙氨酸几乎完全转化为胱氨酸和半胱氨酸(或其S-碱金属或铵盐),半胱氨酸及其盐通过酸处理或氧化反应容易地转化为胱氨酸。