首页> 外国专利> ORTHO-SUBSTITUTED HEYDROXY-PHENYLALKYLENE-CARBOXY-ALKYLENE-1,3,5- TRIAZINES AND THEIR USE AS ANTIOXIDANTS IN SYNTHETIC RESIN COMPOSI TIONS

ORTHO-SUBSTITUTED HEYDROXY-PHENYLALKYLENE-CARBOXY-ALKYLENE-1,3,5- TRIAZINES AND THEIR USE AS ANTIOXIDANTS IN SYNTHETIC RESIN COMPOSI TIONS

机译:邻位取代的羟基-苯-甲醛-羧基-亚烷基-1,3,5-三嗪及其在合成树脂组合物中的抗氧化剂用途

摘要

A process for the preparation of ortho substituted hydroxyphenylalcohylenecarboxyalkohylene-1,3,5-triazines having the general formula: **(See formula)** where n is an integer from 1 to 3; m is an integer from 0 to 3; A1 is selected from the group consisting of alcoholic having 1 to about 4 carbon atoms, and alcohol alcohol, the alcohol having 1 to 14 carbon atoms and the alcohol having 1 to 4 carbon atoms, and imino NHA1; A2 is alcoholic having 1 to about 4 carbon atoms; R2 and R3 are chosen from the group consisting of hydrogen and alcohol having 1 to about 4 carbon atoms, with R2 in the ortho position with respect to the hydroxyl, and R3 being in the ortho or meta position with respect to the hydroxyl; R is bonded to carbon or nitrogen, but in any given triazine all R groups are bonded to either carbon or nitrogen, and when bonded to carbon, R is chosen from the group consisting of oxo, alcohol, aryl, cycloalkoxy, and hydroxyalkoxy, and NHR1, with R1 being chosen from the group consisting of alcohol, cycloalkoxy, or hydroxyalkyl, and when bonded to nitrogen, R is selected from the group consisting of alcohol, cycloalkoxy, aryl, and hydroxyaryl; the alcoholic groups R having from 1 to about 18 carbon atoms, the cycloalkyl groups R having from 3 to about 8 carbon atoms in the ring, any remaining carbon atoms being in ring-bound alcoholic substituents, the aryl groups having R 6 carbon atoms, 10 carbon atoms and 14 carbon atoms, and the alcohol-carboxy-alcohol-hydroxyphenyl groups being attached to carbon or nitrogen, but all of these groups being linked, in any 1,3,5-triazine, to carbon or to nitrogen, which comprises reacting a compound having the formula **(See formula)** with a compound selected from the group consisting of **(See formula)** where R, A1, A2, R2 and R3 are as previously defined. (Machine-translation by Google Translate, not legally binding)
机译:一种具有通式**(见式)**的邻位取代的羟基苯基链烯基羧基亚烷基-1,3,5-三嗪的制备方法,其中n是1至3的整数; m是0至3的整数; A1选自具有1至约4个碳原子的醇和醇,具有1至14个碳原子的醇和具有1至4个碳原子的醇和亚氨基NHA1; A2是具有1至约4个碳原子的醇; R 2和R 3选自氢和具有1至约4个碳原子的醇,其中R 2相对于羟基为邻位,且R 3相对于羟基为邻位或间位。 R与碳或氮键合,但在任何给定的三嗪中,所有R基团均与碳或氮键合,并且当与碳键合时,R选自氧,醇,芳基,环烷氧基和羟基烷氧基,以及NHR1,R1选自醇,环烷氧基或羟烷基,并且当键合至氮时,R选自醇,环烷氧基,芳基和羟芳基;醇基R具有1至约18个碳原子,环烷基R在环中具有3至约8个碳原子,任何剩余的碳原子在环结合的醇取代基中,芳基具有R 6碳原子, 10个碳原子和14个碳原子,并且醇-羧基-醇-羟基苯基基团与碳或氮相连,但所有这些基团在任何1,3,5-三嗪中均与碳或氮相连,包括使具有式**(参见式)**的化合物与选自由**(参见式)**组成的组的化合物反应,其中R,Al,A2,R2和R3如先前所定义。 (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ES398451A1

    专利类型

  • 公开/公告日1975-06-16

    原文格式PDF

  • 申请/专利权人 S. A. ARGUS CHEMICAL N. V.;

    申请/专利号ES19710398451

  • 发明设计人

    申请日1971-12-29

  • 分类号C07D;

  • 国家 ES

  • 入库时间 2022-08-23 04:21:58

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