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CAS No. : | 190723-12-7 | MDL No. : | MFCD08695787 |
Formula : | C6H2Br2O4S | Boiling Point : | No data available |
Linear Structure Formula : | - | InChI Key : | ZZYYIZHQMCEKLG-UHFFFAOYSA-N |
M.W : | 329.95 | Pubchem ID : | 16640107 |
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 |
---|---|---|
at 140℃; for 12h;Inert atmosphere; | Acetic anhydride (7.6 mL) was added to 1 (0.50 g, 1.52 mmol) under a nitrogen atmosphere. The mixture was heated to 140 C for 12 h and then cooled to room temperature. The volatile compounds were removed in vacuo and the crude product was used in the next step without purification. After the brown solid was dissolved in toluene (1 mL), 4-trifluoromethylaniline (294 mg, 1.83 mmol) was added to the solution and the mixture was heated under reflux for 24 h. After removing the volatile components, thionyl chloride was added to the residue and the reaction mixture was stirred at 90 C for 12 h. The volatile components were removed in vacuo and the residue was extracted with chloroform. The organic phase was dried with anhydrous sodium sulfate and the solvent was removed under a reduced pressure. The crude product was purified by column chromatography with silica gel using chloroform as the eluent. The product was recrystallized from ethanol to afford TPD1 as an off-white solid with a yield of 81%. 1H NMR (500 MHz, CDCl3, rt): δ 7.76 (d, J = 8.0 Hz, 2H), 7.55 (d, J = 8.0 Hz, 2H). 13C NMR (125 MHz, CDCl3, rt): δ 158.73, 134.55, 133.86, 130.14, 126.42, 126.26, 126.23, 114.90. Anal. Calcd for C13H4Br2F3NO2S: C, 34.31; H, 0.89; N, 3.08. Found: C, 34.11; H, 0.95; N, 3.06. |
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