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Chemical Structure| 321903-29-1 Chemical Structure| 321903-29-1

Structure of 321903-29-1

Chemical Structure| 321903-29-1

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Product Details of [ 321903-29-1 ]

CAS No. :321903-29-1
Formula : C9H12OSi
M.W : 164.28
SMILES Code : C[Si]1(C)OCC2=CC=CC=C12
MDL No. :MFCD20922818

Safety of [ 321903-29-1 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H227
Precautionary Statements:P501-P210-P264-P280-P302+P352-P370+P378-P337+P313-P305+P351+P338-P362+P364-P332+P313-P403+P235

Application In Synthesis of [ 321903-29-1 ]

* 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 [ 321903-29-1 ]

[ 321903-29-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 853955-69-8 ]
  • [ 15852-73-0 ]
  • [ 69605-90-9 ]
  • [ 321903-29-1 ]
YieldReaction ConditionsOperation in experiment
92%; 68% With potassium carbonate;copper(l) iodide; bis(eta3-allyl-mu-chloropalladium(II)); ruphos; In tetrahydrofuran; N,N-dimethyl-formamide; at 75℃; for 24h;Product distribution / selectivity; Example 6; Method for Preparing Organic Compounds by Using the Silicon-Based Cross-Coupling Reagent 2a of the Present Invention; As expressed by the following reaction formula (Iv), the silicon-based cross-coupling reagent 2a of the present invention was used to prepare various organic compounds by carrying out a cross-coupling reaction between the silicon-based cross-coupling reagent 2a and an organic halide Br-R10. Each of Table 3 and Table 4 shows the organic halide Br-R10, amounts (mmol) of the silicon-based cross-coupling reagent 2a used, reaction times (h), yields of the resultant R1-R10, and yields of oxasilacyclopentane ((11') in the reaction formula (Iv)) generated as a by product.; In the present Example, a mixture of DMF (0.8 mL) and THF (2.2 mL) was used as a solvent. The organic halide Br-R10 (1.0 mmol) was sequentially added to a mixture of the silicon-based cross-coupling reagent 2a, K2CO3 (2.5 mmol), [(eta3-C3H5)PdCl]2 (0.5 mol % with respect to the organic halide), 2-(dicyclohexylphosphino)-2',6'-isopropoxybiphenyl (ligand L: 2.1 mol % with respect to the organic halide), CuI (3 mol % with respect to the organic halide) in the solvent, and the resulting mixture was stirred at 75 C. When each time period shown in Tables 3 and 4 had passed, the resulting mixture was diluted with diethyl ether and was washed with water and brine, and then was dried over anhydrous MgSO4. After concentration with an evaporator, the residue was purified by flash chromatography on silica gel, thereby obtaining organic compounds p51 to p70 which were cross-coupling products respectively corresponding to yields shown in Tables 3 and 4.
 

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