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CAS No. : | 16116-78-2 | MDL No. : | MFCD01863556 |
Formula : | C11H13BrSi | Boiling Point : | No data available |
Linear Structure Formula : | BrC6H4CCSi(CH3)3 | InChI Key : | RNMSGCJGNJYDNS-UHFFFAOYSA-N |
M.W : | 253.21 | Pubchem ID : | 4226980 |
Synonyms : |
|
Signal Word: | Warning | Class: | |
Precautionary Statements: | P261-P305+P351+P338 | UN#: | |
Hazard Statements: | H302-H315-H319-H335 | Packing Group: | |
GHS Pictogram: |
* 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.
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
399 mg | With water; 1,8-diazabicyclo[5.4.0]undec-7-ene; at 20℃; for 30h;Inert atmosphere; Schlenk technique; | PdCl2(PPh3)2 (84 mg, 0.12 mmol,6.0 mol%), CuI (38 mg, 0.20 mmol, 10 mol%) and 1-bromo-4-iodobenzene (566 mg,2.0 mmol, 1.0 equiv) were added into a 30-mL 2-neck round-bottom flask with amagnetic stirring bar. The flask was evacuated and refilled with N2 gas following theusual Schlenk technique. Dry benzene (10 mL) was added while stirring. N2-spargedNEt3 (1.7 mL, 12 mmol, 6.0 equiv) and trimethylsilylacetylene (0.28 mL, 2.0 mmol,1.0 equiv) were added and the reaction flask was wrapped with aluminum foil andstirred at room temperature for 18 h. Iodobenzene (408 mg, 2.0 mmol, 1.0 equiv),DBU (3.6 mL, 24 mmol, 12.0 equiv) and distilled water (14 μL, 0.8 mmol, 40 mol%)were added consecutively and stirring was continued at room temperature foradditional 30 h. The reaction was quenched with water (10 mL) and extracted withdiethyl ether (10 mL). The organic layer was washed with 10% aqueous HCl (3 10mL), brine (20 mL), dried over Na2SO4, gravity-filtered and the solvent removed invacuo. The crude product was purified by silica gel column chromatography inhexane and concentrated in vacuo to obtain 1h in 78% (399 mg, 1.6 mmol) yield ascrystals. |
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