Preparation of 2-pimelie kelone compound

A technology for cyclohexenones and compounds, which is applied in the field of preparation of 2-cyclohexenones, can solve problems such as difficulties in introducing substituents at the 4-position, increased reaction costs, constraints, etc., and achieve high reaction yields. Reduced, wide application prospects, good effect of reaction efficiency
CN101412667BActive Publication Date: 2012-06-27ZHEJIANG UNIV OF TECH

Patent Information

Authority / Receiving Office
CN · China
Patent Type
Patents(China)
Current Assignee / Owner
ZHEJIANG UNIV OF TECH
Publication Date
2012-06-27

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Abstract

The invention discloses a method for preparing 2-cyclohexenone compound, which comprises the following steps: under the action of a metallic catalyst MYn.L, 1, 6-heptadiyne compound showed in formula (I) taken as a raw material is reacted in an ionic liquid at a temperature of between 0 and 150 DEG C; after the reaction liquid is treated, the 2-cyclohexenone compound showed in formula (II) is prepared; and at the same time, the ionic liquid fixed with the metallic catalyst can be recycled. The method has the advantages of simple and reliable operation, high yield and selectivity, repeated recycling and use of the noble metal catalyst, environmental protection, and the like. Because the cyclohexenone compound is a good raw material for synthesizing medicines, pesticides and chemical products, the method has wide industrial application prospect.
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Description

(1) Technical field

[0001] The invention relates to a preparation method of 2-cyclohexenone compounds. (2) Background technology

[0002] Cyclohexenone compounds are very important intermediates in organic synthesis and are used in the fields of medicine, pesticide and chemical industry. Although the synthetic method of multiple 2-cyclohexenone compounds is reported ((1) J.Heterocycl.chem.1972,9,741 at present; (2) J.Am.Chem.Soc.1976,98,4887 ; (3) J.Org.Chem.1977, 42, 1349; (4) Bull.Chem.Soc.Jap.1997, 79, 1879; (5) J.Org.Chem.1997, 62, 9323), but Due to the structural specificity of its functional derivatives, its synthesis is greatly restricted. For example, the synthesis of 4-substituted derivatives of 2-cyclohexenones needs to introduce substituents in advance before ring closure, and at least 4 ~5 steps of chemical reaction can be completed, and the synthesis of such compounds under alkaline conditions will be restricted if the starting material molecule has functional...

Claims

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