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New processes for the preparation of 3-bromoanisole and 3-bromonitrobenzene

机译:制备3-溴茴香醚和3-溴硝基苯的新方法

摘要

Process for the preparation of 3-bromoanisole comprising methoxydenitrating 3-bromonitrobenzene in the presence of a phase-transfer catalyst (PTC), and the preparation of 3-bromonirtobenzene by the bromination of nitrobenzene with bromine in oleum. The methoxydenitration reagent in an alkali metal methoxide, which is selected from sodium methoxide and potassium methoxide. The amount of methoxide used is 1-1.5 mol per mol of 3-bromonitrobenzene. The alkali methoxide can be a pre-prepared solid or it can be prepared in situ, by the reaction of the corresponding alkali hydroxide and methanol. In the case when pre-prepared solid methoxide is used, the effective amount of alkali hydroxide is between 1.2-1.7 mol per mol of 3-bromonitrobenzebe. The reaction temperatures are between about 40 to 80° C., with preference to reaction temperatures of 50 to 55° C. In the case in which methoxide is prepared in situ, the effective amount of alkali hydroxide is between 2.2-2.4 mol per mol of 3-bromonitrobenzene. The reaction temperatures are between about 50 to 80° C. with preference to reaction temperatures of 55 to 65° C.
机译:包括在相转移催化剂(PTC)存在下甲氧基化3-溴硝基苯的3-溴茴香醚的制备方法,以及通过在发烟硫酸中用溴溴化硝基苯来制备3-溴苯甲基苯。碱金属甲醇盐中的甲氧基脱氮试剂,其选自甲醇钠和甲醇钾。每摩尔3-溴硝基苯使用的甲醇盐的量为1-1.5摩尔。碱金属甲醇盐可以是预先制备的固体,也可以通过相应的碱金属氢氧化物与甲醇的反应原位制备。在使用预先制备的固体甲醇盐的情况下,碱金属氢氧化物的有效量为每摩尔3-溴硝基苯泽贝1.2-1.7摩尔。反应温度为约40至80℃,优选为50至55℃。在就地制备甲醇的情况下,碱金属氢氧化物的有效量为每摩尔2.2至2.4摩尔。 3-溴硝基苯。反应温度在约50至80℃之间,优选55至65℃的反应温度。

著录项

  • 公开/公告号AU2954899A

    专利类型

  • 公开/公告日1999-10-25

    原文格式PDF

  • 申请/专利权人 BROMINE COMPOUNDS LTD;

    申请/专利号AU19990029548

  • 发明设计人 MARK GELMONT;JOSEPH ZILBERMAN;

    申请日1999-03-22

  • 分类号C07C43/225;C07C41/01;C07C205/12;C07C201/12;

  • 国家 AU

  • 入库时间 2022-08-22 02:23:07

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