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CAS No. : | 16588-16-2 | MDL No. : | MFCD00219621 |
Formula : | C9H8ClNO4 | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | BLNLZRQIUGDTAO-UHFFFAOYSA-N |
M.W : | 229.62 | Pubchem ID : | 1268247 |
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 |
---|---|---|
94.6% | With potassium carbonate; dimethyl sulfoxide; | EXAMPLE 20 Synthesis of Compound (50), 5-phenyl-(4-ethoxycarbonyl-2-nitrophenyl)-4-isoxazolin-3-one: After mixing 200 g of ethyl 4-chloro-3-nitrobenzoate, 500 ml of dimethyl sulfoxide, 169 g of <strong>[1006-67-3]5-phenylisoxazole</strong>, and 146 g of potassium carbonate, the reaction was performed for 5 hours at 60 C. After the reaction was over, the reaction mixture was cooled and poured into water to deposit crystals which were then recovered, washed with water, and dried to provide 292 g of the desired product with a yield of 94.6%. The melting point thereof was 142 C. to 143 C. |
94.6% | With potassium carbonate; dimethyl sulfoxide; | Synthesis Example 12-1 Synthesis of 5-phenyl-(4-ethoxycarbonyl-2-nitrophenyl)-4-isoxazolin-3-one After mixing 200 g of ethyl 4-chloro-3-nitrobenzoate, 500 ml of dimethyl sulfoxide, 169 g of <strong>[1006-67-3]5-phenylisoxazole</strong>, and 146 g of potassium carbonate, the reaction was performed for 5 hours at 60 C. After the reaction was over, the reaction mixture was cooled and poured into water. Crystals thus deposited were recovered by filtration, washed with water, and dried to provide 292 g of the above-described compound with a yield of 94.6%. The melting point thereof was 142 C. to 143 C. |
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