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filingDate 2018-04-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2021-12-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2021-12-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-110343040-B
titleOfInvention Method for preparing chiral trans-first chrysanthemic acid
abstract The invention provides a method for preparing chiral trans-first chrysanthemic acid, belonging to the field of organic synthesis. The invention relates to a method for synthesizing chiral first chrysanthemic acid by asymmetric cyclopropanation reaction of 2, 5-dimethyl-2, 4-hexadiene and ethyl diazoacetate, and hydrolyzing the chiral first chrysanthemic acid. The chiral copper catalyst is prepared with copper salt and chiral tridentate P, N, N-ligand in situ in various polar and non-polar solvents. The invention can conveniently synthesize the chiral trans-first chrysanthemic acid, and the enantiomeric excess percentage of the chiral trans-first chrysanthemic acid is as high as 95%. The method has the characteristics of simple operation, easily obtained raw materials, wide application range of the substrate, high enantioselectivity and the like.
priorityDate 2018-04-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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