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Chemical Structure| 160194-29-6 Chemical Structure| 160194-29-6

Structure of 4-(Triethylsilyl)but-3-yn-1-ol
CAS No.: 160194-29-6

Chemical Structure| 160194-29-6

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Product Details of [ 160194-29-6 ]

CAS No. :160194-29-6
Formula : C10H20OSi
M.W : 184.35
SMILES Code : OCCC#C[Si](CC)(CC)CC
MDL No. :MFCD00190219
InChI Key :WAVVVDUELKMQAZ-UHFFFAOYSA-N
Pubchem ID :2760694

Safety of [ 160194-29-6 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 160194-29-6 ]

* 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 [ 160194-29-6 ]

[ 160194-29-6 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 160194-29-6 ]
  • [ 211308-79-1 ]
  • 2-(5-Methyl-2-triethylsilanyl-1H-pyrrolo[2,3-b]pyridin-3-yl)-ethanol [ No CAS ]
  • 2
  • [ 220185-63-7 ]
  • [ 160194-29-6 ]
  • [ 1382991-48-1 ]
YieldReaction ConditionsOperation in experiment
100% With sodium carbonate; lithium chloride;(1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; In N,N-dimethyl-formamide; at 100℃; for 15.0h; INTERMEDIATE 51 - PREPARATION of 2-(5,6-Dichloro-2-(triethylsilyl)-1 H-indol-3- yl)ethanol. <strong>[220185-63-7]4,5-Dichloro-2-iodoaniline</strong> (1.50 g; 5.21 mmol), 4-(triethylsilyl)but-3-yn-1-ol (1.65 mL; 7.81 mmol), bis(diphenylphosphino)ferrocene]palladium(ll) chloride (0.212 g; 0.260 mmol), lithium chloride (0.221 g; 5.21 mmol) and sodium carbonate (1.10 g; 10.42 mmol) were suspended in DMF (14 mL) and the mixture was stirred at 100C for 15 hours. The solution was concentrated under reduced pressure and diluted with ethyl acetate. The organic layer was successively washed with brine, sodium thiosulfate, dried and concentrated under reduced pressure. The crude residue was purified by flash chromatography on silica gel (eluent 2 to 20 % ethyl acetate in heptane) to afford 2.0 g (quantitative yield) of the title compound as a brown oil.ESI/APCI(+):344 (M+H); ESI/APCI(-):342 (M-H).
100% With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; sodium carbonate; lithium chloride; In N,N-dimethyl-formamide; at 100℃; for 15.0h; <strong>[220185-63-7]4,5-Dichloro-2-iodoaniline</strong> (1.50 g; 5.21 mmol), 4-(triethylsilyl)but-3-yn-1-ol (1.65 mL; 7.81 mmol), bis(diphenylphosphino)ferrocene]palladium(II) chloride (0.212 g; 0.260 mmol), lithium chloride (0.221 g; 5.21 mmol) and sodium carbonate (1.10 g; 10.42 mmol) were suspended in DMF (14 mL) and the mixture was stirred at 100 C. for 15 hours. The solution was concentrated under reduced pressure and diluted with ethyl acetate. The organic layer was successively washed with brine, sodium thiosulfate, dried and concentrated under reduced pressure. The crude residue was purified by flash chromatography on silica gel (eluent 2 to 20% ethyl acetate in heptane) to afford 2.0 g (quantitative yield) of the title compound as a brown oil. [0645] ESI/APCI(+): 344 (M+H); ESI/APCI(-): 342 (M-H).
 

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