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Antitumor drug intermediates 3, 5-tert-butyl-4-hydroxy benzoic acid synthesis method

机译:抗肿瘤药物中间体3,5-叔丁基-4-羟基苯甲酸的合成方法

摘要

The present invention discloses antitumor drug intermediates 3, 5-tart-butyl-4-hydroxy benzoic acid synthesis method, comprises the following steps:2-amino-3, 5-tort butyl-4-hydroxy-6-benzyl bromide, sodium sulfate solution were added to the reaction vessel, controlled the stirring speed, controlled the temperature of the solution, reacted, added nitro-methane solution, raised the temperature of the solution, stirred speed, continued to react; added diethyl glutarate solution, and niobium pentachloride powder, reacted, washed with the sodium bromide solution for several times, added oxalic acid solution, adjusted the, washed with the 1, 2-diphenyl ethane solution for several times, re-crystallized in the dibutylamine solution, dehydrated with dehydration, got the finished product 3, 5-tert-butyl-4-hydroxy benzoic acid. Figure 1
机译:本发明公开了抗肿瘤药中间体3,5-叔丁基-4-羟基苯甲酸的合成方法,包括以下步骤:2-氨基-3,5-叔丁基-4-羟基-6-苄基溴,硫酸钠将溶液加入反应容器中,控制搅拌速度,控制溶液温度,反应,加入硝基甲烷溶液,升高溶液温度,搅拌速度,继续反应;加入戊二酸二乙酯溶液和五氯化铌粉末,反应,用溴化钠溶液洗涤数次,加入草酸溶液,调节pH,用1,2-二苯乙烷溶液洗涤数次,在二丁胺中重结晶溶液,经脱水脱水,得到最终产物3,5-叔丁基-4-羟基苯甲酸。 <图1>

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