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Chemical Structure| 66117-64-4 Chemical Structure| 66117-64-4

Structure of 66117-64-4

Chemical Structure| 66117-64-4

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Product Details of [ 66117-64-4 ]

CAS No. :66117-64-4
Formula : C14H15BO
M.W : 210.08
SMILES Code : CC1=CC=C(B(O)C2=CC=C(C)C=C2)C=C1
MDL No. :MFCD09972117

Safety of [ 66117-64-4 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319
Precautionary Statements:P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330

Application In Synthesis of [ 66117-64-4 ]

* 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 [ 66117-64-4 ]

[ 66117-64-4 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 6574-97-6 ]
  • [ 66117-64-4 ]
  • [ 1519010-72-0 ]
  • [ 1519010-73-1 ]
  • [ 1519010-71-9 ]
  • 2
  • N-(3,5-bis(trifluoromethyl)phenyl)-4-fluoro-Ntosylbenzamide [ No CAS ]
  • [ 66117-64-4 ]
  • [ 530-46-1 ]
YieldReaction ConditionsOperation in experiment
96% With (bis(tricyclohexyl)phosphine)palladium(II) dichloride; potassium carbonate; tricyclohexylphosphine; In 1,4-dioxane; at 110℃; for 6h;Inert atmosphere; Schlenk technique; General procedure: Under a N2 atmosphere, to a 10 mL dry flask were added amide (0.5 mmol), diarylborinic acid (0.375 mmol), Pd(PCy3)2Cl2 (1 mmolpercent), PCy3 (0.6 mmolpercent), K2CO3 (1 mmol), and dry dioxane (4 mL). The mixture was stirred at 110 °C for a given time or monitored by TLC until the starting material was completely consumed. The reaction mixture was diluted with CH2Cl2 (15 mL), followed by washing with H2O (2 x 10 mL). The organic layer was dried over Na2SO4, filtered, and evaporated under reduced pressure to give crude product,which was purified by column chromatography on silica gel to afford product.
  • 3
  • [ 456-22-4 ]
  • [ 66117-64-4 ]
  • [ 530-46-1 ]
  • 4
  • [ 66117-64-4 ]
  • 4-fluoro-N-methyl-N-tosylbenzamide [ No CAS ]
  • [ 530-46-1 ]
YieldReaction ConditionsOperation in experiment
93% With [1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene](3-chloropyridyl)palladium(ll) dichloride; potassium carbonate; In tetrahydrofuran; at 65℃; for 12h;Inert atmosphere; Schlenk technique; General procedure: Under a N2 atmosphere, to a 10 mL dry flask were added amide (0.5 mmol), diarylborinic acid (1.0 mmol), (IPr)PdCl2(3-chloropydine) (1 molpercent), K2CO3 (1.5mmol), and THF (4 mL). The mixture was stirred at 65°C for a given time or monitored by TLC until the starting material was completely consumed. The reaction mixture was diluted with CH2Cl2 (15 mL), followed by washing with H2O (2×10 mL).The organic layer was dried over Na2SO4, filtered, and evaporated under reduced pressure to give crude product, which was purified by column chromatography on silica gel to afford product.
 

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