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Chemical Structure| 1232892-63-5 Chemical Structure| 1232892-63-5

Structure of 1232892-63-5

Chemical Structure| 1232892-63-5

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Product Details of [ 1232892-63-5 ]

CAS No. :1232892-63-5
Formula : C9H8FNO3
M.W : 197.16
SMILES Code : CC(C1=CC([N+]([O-])=O)=C(C)C=C1F)=O

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Application In Synthesis of [ 1232892-63-5 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 1232892-63-5 ]

[ 1232892-63-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 29427-48-3 ]
  • [ 1232892-63-5 ]
YieldReaction ConditionsOperation in experiment
With copper(II) nitrate; trifluoroacetic anhydride; In chloroform; at 20 - 60℃; Preparation 3; 3-(5-Amino-2-fluoro-4-methyl-phenyl)-5-methyl-pyrazole-1-carboxylic acid benzyl ester; The synthetic procedure used in this preparation is outlined in Scheme C. Step 1; 1-(2-Fluoro-4-methyl-5-nitro-phenyl)-ethanone; Copper (II) nitrate (3.175 g) was added portion wise to a room temperature solution of <strong>[29427-48-3]1-(2-fluoro-4-methyl-phenyl)-ethanone</strong> (2.74 g) in chloroform (30 ml) and Trifluoroacetic anhydride. The mixture was heated at 60 C. for 30 minutes then cooled to room temperature and added to ice. The mixture was extracted with methylene chloride, and the organic layer was washed with water and brine, dried (Na2SO4), filtered and concentrated under reduced pressure to give 3.17 g of 1-(2-Fluoro-4-methyl-5-nitro-phenyl)-ethanone as a reddish oil, which was used directly without further purification.
With copper(II) nitrate; trifluoroacetic anhydride; In chloroform; at 20 - 60℃; Copper (II) nitrate (3.175 g) was added portion wise to a room temperature solution of <strong>[29427-48-3]1-(2-fluoro-4-methyl-phenyl)-ethanone</strong> (2.74 g) in chloroform (30 ml) and Trifluoroacetic anhydride. The mixture was heated at 60 C. for 30 minutes then cooled to room temperature and added to ice. The mixture was extracted with methylene chloride, and the organic layer was washed with water and brine, dried (Na2SO4), filtered and concentrated under reduced pressure to give 3.17 g of 1-(2-Fluoro-4-methyl-5-nitro-phenyl)-ethanone as a reddish oil, which was used directly without further purification.
 

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