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CAS No. : | 98447-30-4 | MDL No. : | MFCD06797977 |
Formula : | C7H6BrNO3 | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | RYKPDLZQIABTMY-UHFFFAOYSA-N |
M.W : | 232.03 | Pubchem ID : | 12966745 |
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 |
---|---|---|
85.0% | With potassium carbonate; In diethyl ether; water; ethyl acetate; N,N-dimethyl-formamide; | Example 2 2-Bromo-4-methoxy-1-nitrobenzene (Compound 5) Compound 4 (2.0 g, 9.22 mmol) was dissolved in DMF (40 mL), and K2CO3 (2.5 g, 18.44 mmol) was added. The reaction mixture was stirred at room temperature for 20 min. After cooling to 0° C., a solution of iodomethane (861 muL, 13.83 mmol) in DMF (5 mL) was added dropwise, and the resulting mixture was stirred at room temperature for 2 h. The reaction was quenched by adding H2O (100 mL) and partitioned with Et2O (200 mL). The organic layer was washed with H2O (3*50 mL) and brine (50 mL). The organic layer was collected, dried over anhydrous Na2SO4, filtered, concentrated, and purified by silica column chromatography (20percent EtOAc in hexanes) to afford compound 5 in 85.0percent (1.81 g) yield as a yellow solid. 1H-NMR (CDCl3, 400 MHz) delta 7.89 (1H, d, J=9.2 Hz, Ar), 7.22 (1H, s, Ar), 6.91 (1H, d, J=9.2 Hz, Ar), 3.89 (3H, s, OCH3); MS (ESI) m/z Calcd for C7H6BrNO3 (M+): 231.0, Found: 232.1 (M+H+). |
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