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METHOD FOR SYNTHESIZING 2,4,6-TRIFLUOROBENZYLAMINE

机译:2,4,6-三氟联苯胺的合成方法

摘要

Disclosed is a method for synthesizing 2,4,6-trifluorobenzylamine, belonging to the technical field of chemical synthesis, and comprising the following steps: (1) reacting pentachlorobenzonitrile as a raw material in 2,4,6-trifluoro-3,5-dichlorobenzonitrile as a solvent with a fluorinating agent for a fluorination reaction to obtain 2,4,6-trifluoro-3,5-dichlorobenzonitrile; (2) subjecting the 2,4,6-trifluoro-3,5-dichlorobenzonitrile obtained in step (1) to reduction by hydrogenation with hydrogen in the presence of an organic carboxylic acid and using palladium charcoal as a catalyst, so as to obtain 2,4,6-trifluoro-3,5-dichlorobenzylamine; and (3) subjecting the 2,4,6-trifluoro-3,5-dichlorobenzylamine obtained in step (2) to reduction by hydrogenation with hydrogen in a solvent under the action of the catalyst, so as to obtain 2,4,6-trifluorobenzylamine. The synthesis method has advantages such as a low raw material cost, a short reaction procedure, a high reaction yield, a good product purity, simple operation, and is suitable for application in industrial production.
机译:本发明公开了一种合成2,4,6-三氟苄胺的方法,属于化学合成技术领域,包括以下步骤:(1)使五氯苄腈为原料在2,4,6-三氟-3,5中反应。以-二氯苄腈为溶剂,与氟化剂进行氟化反应,得到2,4,6-三氟-3,5-二氯苄腈; (2)将步骤(1)中得到的2,4,6-三氟-3,5-二氯苄腈在有机羧酸的存在下用氢进行氢化还原,并以钯炭为催化剂,得到2,4,6-三氟-3,5-二氯苄胺; (3)使步骤(2)中得到的2,4,6-三氟-3,5-二氯苄胺在催化剂的作用下,通过在溶剂中用氢加氢进行还原,从而得到2,4,6。 -三氟苄胺。该合成方法具有原料成本低,反应过程短,反应收率高,产物纯度好,操作简单等优点,适用于工业生产。

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