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method of preparing a continuous low chloride content of benzene chloride by chlorination of toluene to benzylidene

机译:甲苯氯化为亚苄基制取连续低氯含量的苯氯化物的方法

摘要

1376497 Benzotrichloride BAYER AG 20 Oct 1972 [22 Oct 1971 6 June 1972] 48403/72 Heading C2C Benzotrichloride is produced continuously by the steps of: (1) reacting toluene with from 75 to 96% of the stoichiometric quantity of chlorine required for the formation of benzotrichloride, in the presence of light at from 70 to 190‹C. in at least two reaction vessels connected to each other in series; and (2) converting the benzal chloride and residual quantities of benzyl chloride produced in step (1) to benzotrichloride by reacting at 70‹ to 190‹ C. with an excess of chlorine of up to 30% of that required for the reaction with toluene, diluted in an inert gas in at least two reaction vessels connected to each other in series, the ratio of chlorine to inert gas being reduced from in the range of 10 : 1 to 2 : 1 in the first vessel to from 1 : 3 to 1 : 10 in subsequent vessels and the residence times of the reaction mixture in steps 1 and 2 being in the ratio of from 1 : 3 to 1 : 5.
机译:1376497苯并三氯化物BAYER AG 1972年10月20日[1971年10月22日1972年6月6日] 48403/72标题C2C苯并三氯化物是通过以下步骤连续生产的:(1)甲苯与地层所需化学计量的75%至96%的氯反应在70至190°C的光照下检测三苯甲酰氯。在至少两个彼此串联的反应容器中; (2)通过在70℃至190℃下与过量的氯进行反应,将步骤(1)中产生的苯甲酰氯和残余量的苄基氯转化为苯并三氯化物,该氯的量最多为与甲苯反应所需氯的量的30%。在至少两个彼此串联的反应容器中用惰性气体稀释后,氯与惰性气体的比例从第一个容器中的10:1到2:1降低到1:3至在随后的容器中为1:10,步骤1和步骤2中反应混合物的停留时间为1:3至1:5。

著录项

  • 公开/公告号BE790294A

    专利类型

  • 公开/公告日1973-04-19

    原文格式PDF

  • 申请/专利权人 BAYER A.G. A LEVERKUSEN (ALLEMAGNE);

    申请/专利号BED790294

  • 发明设计人

    申请日1972-10-19

  • 分类号C07C;

  • 国家 BE

  • 入库时间 2022-08-23 07:48:33

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