Synthesis method of atorvastatin calcium intermediate 2-chloro-1-(4-fluorophenyl)-2-acetophenone

The invention relates to a novel synthesis method of an atorvastatin calcium intermediate 2-chloro-1-(4-fluorophenyl)-2-acetophenone, and belongs to the technical field of synthesis, and the specific synthesis method comprises the following steps: adding a solvent, a catalyst and a chlorinating agen...

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Bibliographic Details
Main Authors ZHOU TAIYONG, WANG KAI
Format Patent
LanguageChinese
English
Published 01.03.2024
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Summary:The invention relates to a novel synthesis method of an atorvastatin calcium intermediate 2-chloro-1-(4-fluorophenyl)-2-acetophenone, and belongs to the technical field of synthesis, and the specific synthesis method comprises the following steps: adding a solvent, a catalyst and a chlorinating agent into a compound as shown in a formula (3), and reacting at a proper temperature to obtain a compound as shown in a formula (2); adding a solvent, a catalyst and fluorobenzene into the compound in the formula (2), and reacting at a proper temperature to obtain a compound in a formula (1); the preparation method disclosed by the invention is mild in reaction condition, low in cost, safe in process condition, simple in reaction post-treatment and high in product purity, and can fully meet market requirements. 本发明涉及一种阿托伐他汀钙中间体2-氯-1-(4-氟苯基)-2-苯乙酮的合成新方法,属于合成技术领域,具体的合成方法为向式(3)所示的化合物中加入溶剂、催化剂、氯化剂,在适当温度下进行反应,得到式(2)化合物;式(2)化合物中加入溶剂、催化剂、氟苯,在适当温度下进行反应,得到式(1)化合物;本发明所述制备方法反应条件温和,成本低廉,工艺条件安全,反应后处理简单,产品纯度高,能够充分满足市场需求。
Bibliography:Application Number: CN202311352324