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Chemical Structure| 239104-48-4 Chemical Structure| 239104-48-4

Structure of 239104-48-4

Chemical Structure| 239104-48-4

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Product Details of [ 239104-48-4 ]

CAS No. :239104-48-4
Formula : C12H13F3OSi
M.W : 258.31
SMILES Code : FC(F)(F)OC1=CC=C(C#C[Si](C)(C)C)C=C1

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Application In Synthesis of [ 239104-48-4 ]

* 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 [ 239104-48-4 ]

[ 239104-48-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 103962-05-6 ]
  • [ 1066-54-2 ]
  • [ 239104-48-4 ]
YieldReaction ConditionsOperation in experiment
89% With bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; triethylamine; In tetrahydrofuran; at 60℃; for 2h;Inert atmosphere; To a stirred solution of <strong>[103962-05-6]1-iodo-4-(trifluoromethoxy)benzene</strong> (500 mg 1 eq.) in THF (5 ml) under nitrogen, triethylamine (3.5 ml, 3 eq.), trimethylsilyl acetylene (0.731 ml, 3 eq.), Cul (33 mg, 0.1 eq.) and PdCl2(PPh3)2 (122 mg, 0.1 eq.) were added and stirred at 60 C for 2 h. After TLC indicated completion of the reaction, the mixture was filtered through Celite and water (10 ml) was added. The organic phase was extracted by using ethyl acetate (3x 15 ml) and the combined organic phase was washed using brine and dried over sodium sulfate. The solvent was removed to obtain crude product, which was purified by column chromatography to obtain trimethyl-[2-[4-(trifluoromethoxy)phenyl]ethynyl]silane (400 mg, 89% yield). 1H NMR (500 MHz, CDCIs): d 7.29 (d, J = 8.00 Hz, 2H), 6.95 (d, J = 8.00 Hz, 2H), 0.06 (s, 9H).
With copper(l) iodide; triethylamine;trans-bis(triphenylphosphine)palladium dichloride; In tetrahydrofuran; at 20℃; for 3h; To a solution of l-iodo-4-(trifIuoromethoxy)benzene (1.087 mL, 6.94 mMol) and TMS- acetylene (1.166 ml, 8.33 mmol) in THF (30ml) were added Copper(I) iodide (0.066 g, 0.347 mMol), Trans-Bis(triphenylphosphine)palladium(II)chloride (0.244 g, 0.347 mmol) and triethylamine (2.90 ml, 20.83 mmol). After stirring for 3h at room temperature, the reaction mixture was concentrated. The residue was dissolved in heptane, filtered through a plug of silica gel and concentrated to give the desired product as oil. Mass Spectra (m/e): 259 (M+H)
 

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