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CAS No. : | 15362-40-0 | MDL No. : | MFCD00451393 |
Formula : | C14H9Cl2NO | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | JCICIFOYVSPMHG-UHFFFAOYSA-N |
M.W : | 278.13 | Pubchem ID : | 27211 |
Synonyms : |
|
Signal Word: | Warning | Class: | N/A |
Precautionary Statements: | P261-P280-P305+P351+P338 | UN#: | N/A |
Hazard Statements: | H302-H315-H319-H332-H335 | Packing Group: | N/A |
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 dihydrogen peroxide; iron(II); In water; at 20℃;pH 2.0; | General procedure: For the Fenton degradation experiment, 10 mL of a Milli Q water sample acidified at pH 2 with 100 muL H2SO4 0.5 mol/L containing 200 ng of each studied anti-inflammatory drug (diclofenac sodium, ibuprofen and ketoprofen) was placed into a 50 mL brown glass bottle. Immediately, 500 muL of Fe2+solution (1 mg/mL Fe2+) and 200 muL of H2O2 (30percent) were added into the brown bottle which was kept under magnetic stirring and room temperature for different time intervals in order to perform the degradation process. Because the catalyst (Fe2+) and the oxidant (H2O2) are consumed very fast, these were refreshed at each 30 minutes in the same amounts as it was described previously. To study the Fenton oxidative process efficiency over the selected drugs, different experiments at 30, 60 and 120 minutes were performed. After each Fenton oxidative experiment, the degradation by-products of NAIDs were extracted with organic solvent and analyzed by GC×GC-qMS. |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
89% | The compound III (221 g, 0.93 mol) was put into a four-necked flask, and then chloroacetyl chloride (124 g, 1.1 mol) was added in one portion and the temperature was raised to 100 ° C for 3 hours. After cooling, aluminum trichloride (74.5 g, 0.56 mol ), Stir well, then the hydrochloric acid gas absorption system, slowly warming to 100 incubation reaction 1 hour, the reaction slowly poured into 1000ml of water, while stirring side, filter, add a small amount of water to obtain a pale yellow solid 229.6g (Compound IV: 1- (2,6-dichlorophenyl) -2-indolone) in 89percent yield. |
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