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CAS No. : | 153435-79-1 | MDL No. : | MFCD07363818 |
Formula : | C7H8BrNO2S | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | UVSNSICXRVZAJR-UHFFFAOYSA-N |
M.W : | 250.11 | Pubchem ID : | 7213265 |
Synonyms : |
|
Signal Word: | Warning | Class: | N/A |
Precautionary Statements: | P280-P305+P351+P338 | UN#: | N/A |
Hazard Statements: | H302 | Packing Group: | N/A |
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 |
---|---|---|
86% | With dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; cesium fluoride; In 1,2-dimethoxyethane; at 80℃; for 22h;Schlenk technique; Inert atmosphere; | A 15 mL Schlenk tube was dried under vacuum, filled with nitrogen and charged consecutively with 58.9mg (235 μmol, 1.00 eq) 3-bromo-N-methylbenzenesulfonamide (27c), 39.1 mg (235 μmol, 1.00 eq) 4-ethoxyphenylboronic acid, 9.60 mg (12.0 μmol, 0.05 eq) PdCl2(dppf)*DCM, 111 mg (729 μmol, 3.10 eq)CsF and 2.3 mL anhydrous DME. The suspension was stirred at 80 C for 22 h. TLC analysis and GCMSanalysis indicated full conversion of the starting material. The reaction mixture was hydrolyzed byaddition of 10 mL 5% aqueous HCl solution and diluted with 10 mL EtOAc. The layers were separatedand the organic layer was washed with 8 mL 5% aqueous HCl solution, dried over MgSO4 andconcentrated under reduced pressure. Final purification via column chromatography (CH/EtOAc 3:1,size: 17.5 x 2.0 cm, 14 g silica gel) yielded the pure product as beige solid (57 mg, 86 %). |
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