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CAS No. : | 24100-18-3 | MDL No. : | MFCD01570896 |
Formula : | C6H6BrNO | Boiling Point : | No data available |
Linear Structure Formula : | - | InChI Key : | PDOWLYNSFYZIQX-UHFFFAOYSA-N |
M.W : | 188.02 | Pubchem ID : | 90364 |
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 |
---|---|---|
64% | at 0 - 55℃; for 1.5 h; | 2-Amino-5.6-dimethoxypyridine(a) 2-Bromo-3 -methoxy-6-nitropyridine2-Bromo-3-methoxypyridine (4.45 g, 23.7 mmol) was added to a mixture of fuming HNO3 and concentrated H2SO4 (1:1, 18 mL) at O0C. The mixture was stirred at 55°C for 1.5 h and then poured into ice water (150 mL). The precipitate formed was the pure product, which was used without further purification. Yield: 3.54 g (64percent) of slightly yellow solid.1HNMR (DMSOd6, 400 MHz) δ 8.41 (d, IH), 7.80 (d, IH), 4.06 (s, 3H). |
64% | With sulfuric acid; nitric acid In water at 0 - 55℃; for 1.5 h; | 2-Bromo-3-methoxypyridine (4.45 g, 23.7 mmol) was added to a mixture of fuming HNO3 and concentrated H2SO4 (1:1, 18 mL) at 0 0C. The mixture was stirred at 55 0C for 1.5 h and then poured into ice water (150 mL). The precipitate formed was filtered off, washed with water (3x100 mL) and dried in vacuo to give 3.54 g (64percent) of slightly yellow solid, which was essentially pure product. 1HNMR (DMSO-de, 400 MHz) δ 8.41 (d, IH), 7.80 (d, IH), 4.06 (s, 3H). |
60 mg | at 55℃; for 3 h; | To a solution of 2-bromo-3-methoxypyridine (0.1 g) in conc. sulfuric acid (2 mL) wasadded nitric acid (0.1 g). The mixture was stirred at 55°C for 3 hours. After cooling, the mixturewas poured into water (10 mL). The mixture was filtered. The solid was washed with water,and then redissolved in DCM. The solution was dried over Na2SO4 and concentrated in vacuo to afford 2-bromo-3-methoxy-6-nitropyridine (60 mg). MS(ES) m/z 233 (MH). |
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