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Antimalarial medicine intermediates 2,4-dichlorobenzoic acid synthesis method

机译:抗疟药中间体2,4-二氯苯甲酸的合成方法

摘要

#$%^&*AU2018100397A420180517.pdf#####5 Abstract Antimalarial medicine intermediates 2,4-dichlorobenzoic acid synthesis method, comprises the following steps: 4-5 mol N, N-dimethylacetamide solution, 3-4 mol 5 boron trifluoride acetic acid powder were added to the reaction vessel, and the stirring speed was maintained at 90-110 rpm for 30-40 minutes, 2 mol 2,4-dichloro-6-amino-isobutylbenzene solution was added, raised the temperature of the solution to 40-50'C, kept for 100-130 min, continued to raise the temperature to 60-70 C, kept for 30-40 min, filtrated and the precipitation was washed with 10 1-chloro-2-methylpropane solution, the filtrate and the washing liquid were combined, the oxalic acid solution was added to adjust the pH to 4-5, reduced the solution temperature to 10-15 'C, precipitated the crystal, filter it and dehydrated with the dehydration, got finished product 2, 4 - dichlorobenzene formic acid.
机译:#$%^&* AU2018100397A420180517.pdf #####5抽象抗疟药中间体2,4-二氯苯甲酸的合成方法,包括以下步骤:4-5 mol N,N-二甲基乙酰胺溶液,3-4 mol向反应容器中加入5份三氟化硼乙酸粉末,并进行搅拌。速度在90-110 rpm下保持30-40分钟,2 mol加入2,4-二氯-6-氨基-异丁苯溶液,升高温度将溶液升至40-50'C,保持100-130分钟,继续将温度升至60-70°C,保持30-40分钟,过滤,并用合并10份1-氯-2-甲基丙烷溶液,滤液和洗涤液,加入草酸溶液调节pH至4-5,还原溶液温度升至10-15摄氏度,沉淀出晶体,过滤并用硫酸镁脱水脱水,得成品2,4-二氯苯甲酸。

著录项

  • 公开/公告号AU2018100397A4

    专利类型

  • 公开/公告日2018-05-17

    原文格式PDF

  • 申请/专利权人 CHENGDU ZHONG HENG HUA TIE TECHNOLOGY CO. LTD.;

    申请/专利号AU20180100397

  • 发明设计人 PENG XIANGLIANG;

    申请日2018-03-29

  • 分类号C07C51;

  • 国家 AU

  • 入库时间 2022-08-21 12:44:56

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