Preparation method of valproic acid
The invention belongs to the technical field of medicines, and particularly relates to a valproic acid preparation method which comprises the following steps: under the catalysis of heteropoly acid, malonic acid and acetone react in acetic anhydride to obtain malonic acid cyclic isopropyl ester; the...
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Format: | Patent |
Sprache: | chi ; eng |
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Zusammenfassung: | The invention belongs to the technical field of medicines, and particularly relates to a valproic acid preparation method which comprises the following steps: under the catalysis of heteropoly acid, malonic acid and acetone react in acetic anhydride to obtain malonic acid cyclic isopropyl ester; the preparation method comprises the following steps: under the catalysis of a phase transfer catalyst and potassium carbonate, carrying out a reaction on malonic acid cyclic isopropyl ester and halogenated propane, recovering a solvent after the reaction is completed, then adding alkali for hydrolysis, and then adding acid for neutralization to obtain 2, 2-dipropylmalonic acid; 2, 2-dipropylmalonic acid is heated for decarboxylation, and valproic acid is obtained; the whole reaction operation is green, environment-friendly, safe and simple, and the obtained product is high in yield and purity.
本发明属于医药技术领域,具体是涉及一种丙戊酸的制备方法,步骤为,在杂多酸催化下,丙二酸和丙酮在醋酸酐中进行反应,得到丙二酸环异丙酯;在相转移催化剂和碳酸钾催化下,丙二酸环异丙酯和卤代丙烷反应,反应完毕后回收溶剂,然后先加碱水解,再加酸中和,得到2,2 |
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