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Preparation of chiral alpha-hydroxy-amides and carboxylic acids by controlled hydrolysis of corresponding hydroxynitriles with hydrochloric acid in carboxylic acid solvent

机译:通过在羧酸溶剂中用盐酸控制相应的羟基腈水解,制备手性α-羟基酰胺和羧酸

摘要

Method for preparing alpha -hydroxyamides or carboxylic acids (I) comprises reacting the corresponding hydroxynitrile (II) with hydrochloric acid in a 1-6C carboxylic acid solvent. Method for preparing alpha -hydroxyamides or carboxylic acids of formula (I) comprises reacting the corresponding hydroxynitrile of formula (II) with hydrochloric acid in a 1-6C carboxylic acid solvent, using either 25-37% HCl at 0-50 [deg] C to produce amides or 5-25% HCl at 20-100 [deg] C to produce acids. [Image] R1, R21-20C alkyl, 5-20C (hetero)aryl, 7-20C alkylaryl, 5-20C alkylheteroaryl or aralkyl, or 5-20C (alkyl)heterocycle (all optionally substituted once or multiple times); or R1+R2optionally substituted 4-20C alkylene optionally containing 1 or more heteroatoms; or one of R1 and R2 may : H; and X : NH2 or OH.
机译:制备α-羟基酰胺或羧酸(I)的方法包括在1-6C的羧酸溶剂中使相应的羟基腈(II)与盐酸反应。制备式(I)的α-羟基酰胺或羧酸的方法包括在1-6C的羧酸溶剂中,使用25-37%的HCl在0-50℃下,使相应的式(II)的羟基腈与盐酸反应。 C在20-100℃下产生酰胺或5-25%HCl以产生酸。 [图片] R1,R21-20C烷基,5-20C(杂)芳基,7-20C烷基芳基,5-20C烷基杂芳基或芳烷基,或5-20C(烷基)杂环(全部任选地被取代一次或多次);或R 1 + R 2任选取代的4-20C亚烷基,其任选地含有1个或多个杂原子;或R1和R2之一可以:H; X:NH 2或OH。

著录项

  • 公开/公告号AT413100B

    专利类型

  • 公开/公告日2005-11-15

    原文格式PDF

  • 申请/专利权人 DSM FINE CHEMICALS AUSTRIA NFG GMBH & CO KG;

    申请/专利号AT20030000937

  • 发明设计人

    申请日2003-06-17

  • 分类号C07B41/08;C07B43/06;

  • 国家 AT

  • 入库时间 2022-08-21 21:36:16

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