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Drug intermediates p-benzoylbenzoic acid synthesis method

机译:药物中间体对苯甲酰苯甲酸的合成方法

摘要

The present invention discloses p-benzoylbenzoic acid synthesis method, comprises the following steps: 3-amino-4-hydroxymethylbenzophenone and potassium nitrate solution were added to the reaction vessel, controlled the stirring speed, raised the temperature of the solution, added 2-methyl-l-butanol solution, added terbium oxide powder in batches; maintain reflux, added potassium bromide solution, precipitateed the crystals, filter, washed with o-xylene solution for several times, washed with hexachloroethane solution for several times, recrystallized in thionyl chloro solution, dehydrated with dehydration, got the finished product of p-benzoylbenzoic acid. Figure 1
机译:本发明公开了对苯甲酰苯甲酸的合成方法,包括以下步骤:将3-氨基-4-羟甲基二苯甲酮和硝酸钾溶液加入反应容器中,控制搅拌速度,升高溶液温度,加入2-甲基苯甲酸。 -l-丁醇溶液,分批加入氧化ter粉;保持回流,加入溴化钾溶液,沉淀出晶体,过滤,用邻二甲苯溶液洗涤数次,用六氯乙烷溶液洗涤数次,在亚硫酰氯溶液中重结晶,脱水脱水,得到对苯甲酰苯甲酸的最终产物。酸。 <图1>

著录项

  • 公开/公告号IES20180113A2

    专利类型

  • 公开/公告日2019-11-13

    原文格式PDF

  • 申请/专利权人 CHENGDU QIE SI TE TECHNOLOGY CO. LTD.;

    申请/专利号IE2018S000113

  • 发明设计人 FEI PENG;

    申请日2018-04-04

  • 分类号C07C51;

  • 国家 IE

  • 入库时间 2022-08-21 11:17:20

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