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CAS No. : | 142738-94-1 | MDL No. : | MFCD01631504 |
Formula : | C8H7F3O2 | Boiling Point : | No data available |
Linear Structure Formula : | - | InChI Key : | OKSRAPDSZKICKZ-UHFFFAOYSA-N |
M.W : | 192.14 | Pubchem ID : | 2777188 |
Synonyms : |
|
Signal Word: | Warning | Class: | |
Precautionary Statements: | P261-P301+P312-P302+P352-P304+P340-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 |
---|---|---|
With potassium carbonate; In water; ethyl acetate; N,N-dimethyl-formamide; at 0 - 20℃; for 13.5h; | To a suspension of 20.0 g of <strong>[827-99-6]3-(trifluoromethoxy)phenol</strong> and 23.3 g of K2CO3 (anhydrous) in DMF (100 ml) was added 23.9 g of iodine methane under ice cooling, then the reaction mixture was warmed to room temperature, and was stirred at room temperature for 13 hours. To the reaction solution was added EtOAc (100 ml) and purified water (150 ml), and the resulting mixture was stirred for 30 minutes. After liquid separation, the aqueous layer was extracted with EtOAc (50 ml×2), the combined organic layer was washed with purified water (100 ml×3) and with saturated brine (50 ml) and dried overover MgSO4, then, the drying agent was separated by filtration, and the solvent was removed under reduced pressure to obtain 27.7 g of the title compound (crude form, yellow oil). The present compound was used in the next reaction without purification.MS (CI pos.) m/z: 193 ([M+H]+)1H-NMR (300 MHz, CDCl3) delta (ppm); 3.81 (s, 3H), 6.73-6.87 (m, 3H), 7.25-7.32 (m, 1H) |
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