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通过溴化-脱溴顺序方法合成溴代噻唑。

Synthesis of Brominated Thiazoles via Sequential Bromination-Debromination Methods.

机构信息

Department of Chemistry and Biochemistry, North Dakota State University , NDSU Department 2735, P.O. Box 6050, Fargo, North Dakota 58108-6050, United States.

出版信息

J Org Chem. 2017 Jun 2;82(11):5947-5951. doi: 10.1021/acs.joc.7b00495. Epub 2017 May 16.

Abstract

The synthesis of the full family of bromothiazoles has been revisited in order to update and optimize their production. The species reported include 2-bromothiazole, 4-bromothiazole, 5-bromothiazole, 2,4-dibromothiazole, 2,5-dibromothiazole, 4,5-dibromothiazole, and 2,4,5-tribromothiazole, the majority of which are produced via sequential bromination and debromination steps. This complete family can now be produced without the use of elemental bromine, and the presented methods have allowed the physical and NMR spectroscopic characterization of the full family to be reported for the first time.

摘要

为了更新和优化它们的生产,我们重新研究了全族溴噻唑的合成方法。报道的物种包括 2-溴噻唑、4-溴噻唑、5-溴噻唑、2,4-二溴噻唑、2,5-二溴噻唑、4,5-二溴噻唑和 2,4,5-三溴噻唑,其中大多数是通过顺序溴化和脱溴化步骤生产的。现在,不需要使用元素溴就可以生产出这个完整的家族,所提出的方法还首次允许对全族进行物理和 NMR 光谱学的表征。

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