首页> 外国专利> Method of obtaining acid 4- (para-amino methyl) benzoic understanding the preparation of the catalyst for one of the phases. (Machine-translation by Google Translate, not legally binding)

Method of obtaining acid 4- (para-amino methyl) benzoic understanding the preparation of the catalyst for one of the phases. (Machine-translation by Google Translate, not legally binding)

机译:获得酸4-(对氨基甲基)苯甲酸的方法应理解用于其中一相的催化剂的制备。 (通过Google翻译进行机器翻译,没有法律约束力)

摘要

Process for obtaining 4 (para-amino methyl) benzoic acid comprising the preparation of the catalyst for one of the phases, characterized in that it prevents the separation of the process in two phases of operations, of which the first part of the para-amino benzoic acid and it ends in the obtaining of the 4-cyano benzoic acid and the second part of the result of the previous one and it ends in the 4 (para-amino methyl) benzoic acid and because in the first phase mentioned, molybdenum trisulfide is used as a transformation reagent and in the second, catalytic hydrogenation is used by using a catalyst prepared starting from an 8% solution of freshly prepared sodium hydroxide with a temperature maintained at 50 + 2ºC 6.2% of an alloy is added slowly to equal parts of nickel and aluminum, which is conveniently washed with distilled water and four alcohol traps of 96º and one end of absolute alcohol and preserved in absolute alcohol medium in refrigerator. (Machine-translation by Google Translate, not legally binding)
机译:获得4-(对氨基甲基)苯甲酸的方法,包括制备用于一个相的催化剂,其特征在于,它防止该方法在两个操作阶段中分离,其中对氨基的第一部分苯甲酸,它以得到4-氰基苯甲酸和第二部分的结果为结尾,并且以4-(对氨基甲基)苯甲酸为结尾,并且因为在第一阶段中提到了三硫化钼用作转化试剂,第二种方法是使用催化剂氢化,方法是使用从8%的新鲜制备的氢氧化钠溶液(温度保持在50 +2ºC)开始制备的催化剂,将6.2%的合金缓慢加入等份镍和铝,可以方便地用蒸馏水和四个96º的酒精捕集阱和一个末端的纯酒精洗涤,并保存在冰箱的纯酒精介质中。 (通过Google翻译进行机器翻译,没有法律约束力)

著录项

  • 公开/公告号ES355071A1

    专利类型

  • 公开/公告日1969-11-16

    原文格式PDF

  • 申请/专利号ES19680355071

  • 发明设计人

    申请日1968-06-15

  • 分类号A61K;

  • 国家 ES

  • 入库时间 2022-08-23 11:27:50

相似文献

  • 专利
  • 外文文献
获取专利

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号