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CAS No. : | 126917-10-0 | MDL No. : | MFCD00061155 |
Formula : | C8H3ClF4O | Boiling Point : | - |
Linear Structure Formula : | ClCOC6H3(F)CF3 | InChI Key : | OOAHPLWBUUTFMV-UHFFFAOYSA-N |
M.W : | 226.56 | Pubchem ID : | 145580 |
Synonyms : |
|
Signal Word: | Danger | Class: | 8 |
Precautionary Statements: | P280-P305+P351+P338-P310 | UN#: | 3265 |
Hazard Statements: | 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 |
---|---|---|
47% | With dmap; triethylamine; In tetrahydrofuran; at 20℃; for 3h;Cooling with ice; | Example 1-1 (0142) Production Method of 2-fluoro-N-methyl-4-(trifluoromethyl)-N-(5-(trifluoromethyl)pyridin-2-yl)benzamide (0143) 2-Fluoro-4-trifluoromethyl benzoyl chloride (409 mg) and a THF (1 mL) solution were added to a mixture of <strong>[937602-15-8]N-methyl-5-(trifluoromethyl)pyridin-2-amine</strong> (264 mg), THF (4 mL) and triethylamine (1 mL) under ice cooling. After heating to room temperature, N,N-dimethyl aminopyridine (50 mg) was added, and the resulting mixture was stirred for 3 hours. Water was added to the reaction mixture, and extraction with ethyl acetate was performed. The organic layer was dried over anhydrous magnesium sulfate and then concentrated in vacuo. The resulting residue was subjected to column chromatography to give the desired compound (260 mg, yield: 47%). |
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