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Excepted Quantity | USD 0.00 |
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CAS No. : | 13333-97-6 | MDL No. : | MFCD00068896 |
Formula : | C7H5F3S | Boiling Point : | No data available |
Linear Structure Formula : | - | InChI Key : | XVGQHRKNXSUPEF-UHFFFAOYSA-N |
M.W : | 178.17 | Pubchem ID : | 2777889 |
Synonyms : |
|
Signal Word: | Danger | Class: | 6.1 |
Precautionary Statements: | P501-P261-P270-P271-P264-P280-P337+P313-P305+P351+P338-P361+P364-P332+P313-P301+P310+P330-P302+P352+P312-P304+P340+P311-P403+P233-P405 | UN#: | 2810 |
Hazard Statements: | H301+H311+H331-H315-H319 | Packing Group: | Ⅲ |
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 |
---|---|---|
82.3% | With potassium carbonate; In N,N-dimethyl-formamide; at 100℃; for 3.5h; | N*3*-[3,5-Dichloro-4-(2 rifluoromethyl^henylsulfanyl)^henyl]-lH-[l,2,4]triazole-3,5- iamine (Compound 10) In a 250-mL round-bottomed flask, l,3-dichloro-2-fluoro-5-nitrobenzene (1.22 g, 5.81 mmol, Eq: 1.00), 2-(trifluoromethyl)benzenethiol (1.01 g, 5.67 mmol, Eq: 0.976) and potassium carbonate (0.98 g, 7.09 mmol, Eq: 1.22) were combined with N,N-dimethylformamide (22 mL) to give a light brown suspension. The reaction mixture was heated at 100 C for 3.5 hrs. After this time, the reaction mixture was partitioned between ethyl acetate and water. The organic phase was dried over sodium sulfate, filtered, and concentrated to a brown oil. This crude product was dissolved in methylene chloride, then the mixture was concentrated over silica gel. The silica gel supported crude product was loaded onto a 120 gram silica gel column. Flash chromatography (100% hexanes ramped to 5% ethyl acetate in hexanes) provided 1.76 g (82.3%) of (2,6- dichloro-4-nitrophenyl)(2-(trifluoromethyl)phenyl)sulfane as a light yellow solid. |
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