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CAS No. : | 2363-16-8 | MDL No. : | MFCD00553089 |
Formula : | C8H6BrNO4 | Boiling Point : | No data available |
Linear Structure Formula : | - | InChI Key : | BNNDHGPPQZVKMX-UHFFFAOYSA-N |
M.W : | 260.04 | Pubchem ID : | 2736829 |
Synonyms : |
|
Signal Word: | Warning | Class: | |
Precautionary Statements: | P261-P305+P351+P338 | UN#: | |
Hazard Statements: | 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 |
---|---|---|
100% | With caesium carbonate;tris-(dibenzylideneacetone)dipalladium(0); 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; In 1,4-dioxane; at 95℃; for 16h; | 1.00 g (3.85 mmol) methyl 4-bromo-3-nitro-benzoate are dissolved in 6 ml dioxane with 389 mg (3.85 mmol) <strong>[109-11-5]morpholin-3-one</strong> under a nitrogen atmosphere and 36.6 mg (40 μmol) tris-(dibenzylideneacetone)-dipalladium(0), 67.1 mg (116 μmol) xantphos and 1.75 g (5.38 mmol) caesium carbonate are added. Under a nitrogen atmosphere and with stirring, the reaction mixture is heated to 95 C. for 16 hours. Then it is filtered, the solution is evaporated down i. vac. and evaporated with ether. The residue is further reacted without any more purification. Yield: 1.31 g (quantitative). C12H12N2O6 (280.24) Mass spectrum: (M+H)+=281 Rf value: 0.47 (Reversed phase 8; methanol/5% sodium chloride solution=6:4) |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With tetrakis(triphenylphosphine) palladium(0); sodium carbonate; In 1,4-dioxane; water; at 100℃; for 0.5h;Inert atmosphere; | A mixture of the methyl ester (0.5 g, 1.9 mmol) in Dioxane, boronic acid (0.51 g,2.3 mmol) and a 2M aqueous solution of Na2CO3 was added to a 50 mL RB flaskand the flask was purged with N2 for 15 min. Pd(PPh3)4 (0.10 g, 0.09 mmol) wasadded and the reaction mixture was slowly heated up to 100 °C and stirred for 30 minutes. The reaction mixture was poured in ice water and extracted with EtOAc.The crude material was purified by flash column chromatography (silica gel,Silica Flash?-Silicycle) using EtOAc:Hexane (1:1) to give the product as an offwhitesolid which after characterization was used in the following steps GeneralProcedures B and C. |
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