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CAS No. : | 140690-56-8 | MDL No. : | MFCD00010306 |
Formula : | C9H5BrF6 | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | SWFFFUJOWAJJCH-UHFFFAOYSA-N |
M.W : | 307.03 | Pubchem ID : | 518871 |
Synonyms : |
|
Signal Word: | Danger | Class: | 8,3 |
Precautionary Statements: | P280-P305+P351+P338-P310 | UN#: | 2920 |
Hazard Statements: | H225-H314 | Packing Group: | Ⅱ |
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 |
---|---|---|
91% | Reference Example 53 3-[2,4-bis(trifluoromethyl)benzyl]oxy}-2-methoxybenzaldehyde; [Show Image] To a solution (16 mL) of <strong>[66495-88-3]3-hydroxy-2-methoxybenzaldehyde</strong> (1.00 g) in N,N-dimethylformamide was added potassium carbonate (1.37 g), and the mixture was stirred at room temperature for 0.5 hr. To the reaction mixture was added a solution (2 mL) of 1-(bromomethyl)-2,4-bis(trifluoromethyl)benzene (2.29 g) in N,N-dimethylformamide, and the mixture was stirred at room temperature for 3 days. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and saturated brine, dried over anhydrous magnesium sulfate, and filtered, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate=100:0→90:10) to give the title compound as a pale-yellow oil (yield: 2.27 g, 91%). 1H-NMR (DMSO-d6, 300 MHz):δ3.92 (3H, s), 5.44 (2H, s), 7.20-7.29 (1H, m), 7.36 (1H, dd, J = 7.9, 1.6 Hz), 7.49 (1H, dd, J = 8.0, 1.6 Hz), 8.10 (1H, d, J = 8.3 Hz), 8.14 (1H, s), 8.20 (1H, d, J = 8.3 Hz), 10.32 (1H, s). |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
5.1 g | Weigh 6.10g of <strong>[436-77-1]fangchinoline</strong> dissolved in 100mL of dichloromethaneIn a 500 mL three-necked flask,Add diethylamine10 mL, 2,4-bis(trifluoromethyl)benzyl bromide 3.10 g,Stirring, heat-reacting at 60 C for 12 h, TLC detection of anti-chinolineReaction, distill off dichloromethane, cool to room temperature, neutralize to neutral with 10% hydrobromic acid, dissolve with 200 mL of water, and use 500 g of Treatment with H-type 732 cationic resin, washing with water and then eluting with dilute ammonia water, collecting the fractions containing the product, and steaming under reduced pressure to the liquid volumeAbout 50mL, crystallized at room temperature overnight, filtered, TLC tracking reaction and product separation and purification process, solids dried at 60 C4h, the product was obtained as a yellow powder, 5.10g. |
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