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Chemical Structure| 357274-85-2 Chemical Structure| 357274-85-2

Structure of 357274-85-2

Chemical Structure| 357274-85-2

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Product Details of [ 357274-85-2 ]

CAS No. :357274-85-2
Formula : C3H4BF3O2
M.W : 139.87
SMILES Code : C=C(B(O)O)C(F)(F)F
MDL No. :MFCD03452762

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Application In Synthesis of [ 357274-85-2 ]

* 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 [ 357274-85-2 ]

[ 357274-85-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1160573-64-7 ]
  • [ 357274-85-2 ]
  • [ 1364674-30-5 ]
YieldReaction ConditionsOperation in experiment
With potassium carbonate;bis-triphenylphosphine-palladium(II) chloride; In tetrahydrofuran; water; for 3.0h;Inert atmosphere; Reflux; l-bromo-3,5-dichloro-2-fluorobenzene (10 g), (3,3,3-trifluoroprop-l-en-2-yl)-boronic acid (7.5 g:) and potassium carbonate (13.6 g) were dissolved in tetrahydrofuran (41 ml) and water (20 ml), and then deaerated. Dichlorobis(triphenylphosphine)palladium (II) ( 1.4 g) was added thereto and the mixture was stirred for 3 hours under reflux under argon atomosphere. After cooling the mixture to the room temperature, water and n-hexane were added, and the organic layer was washed with water and dried over anhydrous magnesium sulfate. The drying agent was filtered off, the solvent was distilled off under reduced pressure, and the residue was roughtly purified by silica gel chromatography (n-hexane) to obtain a mixture containing l,3-dichloro-2,4-difluoro-5-(3,3,3-trifluoroprop-l-en-2-yl)benzene and hexane. i-NMR (CDC13) δ: 5.82 (1H, s), 6.25 (1H, s), 7.21-7.26 (1H, m), 7.48-7.43 (1H, m).
With bis-triphenylphosphine-palladium(II) chloride; potassium carbonate; In tetrahydrofuran; water; for 3.0h;Inert atmosphere; Reflux; 1-Bromo-3,5-dichloro-2-fluorobenzene (10 g), (3,3,3-trifluoroprop-1-en-2-yl)-boronic acid (7.5 g:) andpotassium carbonate (13.6 g) were dissolved in tetrahydrofuran (41 ml) and water (20 ml), and then deaerated. Dichlorobis(triphenylphosphine)palladium (II) (1.4 g) was added thereto and the mixture was stirred for 3 hours under reflux under argon atomosphere. After cooling the mixture to the room temperature, water and n-hexane were added, and the organic layer was washed with water and dried over anhydrous magnesium sulfate. The drying agent was filtered off, the solvent was distilled off underreduced pressure, and the residue was roughly purified by silica gel chromatography (n-hexane) to obtain a mixture containing 1,3-dichloro-2,4-difluoro-5-(3,3,3-trifluoroprop-1-en-2-yl)benzene and hexane. 1H-NMR (CDCl3) 5: 5.82 (1H, s), 6.25 (1H, s), 7.21-7.26 (1H, m), 7.48-7.43 (1H, m).
 

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