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CAS No. : | 607-24-9 | MDL No. : | MFCD00003956 |
Formula : | C10H7NO3 | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | MUCCHGOWMZTLHK-UHFFFAOYSA-N |
M.W : | 189.17 | Pubchem ID : | 69083 |
Synonyms : |
|
Signal Word: | Warning | Class: | N/A |
Precautionary Statements: | P261-P305+P351+P338 | UN#: | N/A |
Hazard Statements: | H315-H319-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 |
---|---|---|
65% | Triton-X 405; at 130.0℃; for 3.0h;Product distribution / selectivity; | Surfactant mediated solvent-free protocols were also successfully extended to the conversion of aryl nitro compounds to aryl acetamides. Thus, solvent-free acetamidation reactions involved treating a mixture of the aryl nitro compound (1 eq) with potassium thioacetate (4 eq.) in presence of dry Triton-X 405 (cat) at about 130 DEG C for about 3 hours producing the corresponding arylacetamide in greater than about 95% conversion (HPLC and GC) and selectivity. Representative results for acetamidation of aryl nitro compounds are summarized in Table 2. The general reaction for the acetamidation of the aryl nitro compound is as follows: |
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