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Flavones glycoside drug intermediates acetylene carboxylic acid synthesis method

机译:黄酮糖苷药物中间体乙炔羧酸的合成方法

摘要

The present invention discloses flavones glycoside drug intermediates acetylene carboxylic acid synthesis method, comprises the following steps: 3-propargyl, sodium nitrate solution were added to the reaction vessel, controlled the stirring speed, controlled the temperature of the solution, reacted, added ethyl tert butyl ether solution, raised the temperature of the solution, reacted., added antimony pentachloride powder, and dihydrin diacetate solution, raised the temperature of the solution, continued to react, extracted several times with ethyl tert butyl ether solution, set aside, solution stratification, separated reservoir, washed with the potassium chloride solution for several times, washed with the 3-methyl-2-amyl ketone solution for several times, washed with the dipropylene glycol solution for several times, re-crystallized in the 1, 3-dimethylcyclohexane solution, dehydrated with dehydration, got the finished product acetylene carboxylic acid.
机译:本发明公开了黄酮糖苷药物中间体乙炔羧酸的合成方法,包括以下步骤:将3-炔丙基,硝酸钠溶液加入反应容器中,控制搅拌速度,控制溶液温度,反应后,加入乙基叔胺丁基醚溶液,升高溶液温度,进行反应。,添加五氯化锑粉末和二元醇二乙酸盐溶液,升高溶液温度,继续反应,用乙基叔丁基醚溶液萃取数次,静置,溶液分层,分离出容器,用氯化钾溶液洗涤数次,用3-甲基-2-戊基酮溶液洗涤数次,用二丙二醇溶液洗涤数次,在1,3-二甲基环己烷中重结晶。溶液,经脱水脱水,得到成品乙炔羧酸。

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