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CAS No. : | 5344-49-0 | MDL No. : | MFCD00100425 |
Formula : | C7H4ClNO4 | Boiling Point : | No data available |
Linear Structure Formula : | - | InChI Key : | JYHOMEFOTKWQPN-UHFFFAOYSA-N |
M.W : | 201.56 | Pubchem ID : | 79287 |
Synonyms : |
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Signal Word: | Warning | Class: | |
Precautionary Statements: | P280-P305+P351+P338 | UN#: | |
Hazard Statements: | H302 | 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 |
---|---|---|
90.86% | The compound 2-chloro-6-nitrobenzoic acid (806 mg, 4.0 mmol) was suspended in toluene (10 mL) and then suspended at room temperatureSOCl2 (952 mg, 8.0 mmol) was added in one portion to the reaction solution. The reaction solution was heated to 110 ° C and stirred for 9 hours. The solution was concentrated under reduced pressure. The resulting yellow oil was dissolved in 1,4-dioxane 10 mL) to give a yellow suspension.The compound(1R, 2S) -2-fluorocyclopropylamine tosylatesalt(1.0 g, 4.0 mmol) and NaHCO3 (1.34 g,16.0 mmol) was suspended in 1,4-dioxane (10 mL), and then the yellow suspension obtained above was added dropwise to the reaction solution at 5 ° C. The reaction solution was stirred at room temperature overnight and then diluted with 100 mL of water, The resulting mixture was extracted with ethyl acetate (50 mL x 3), the combined organic phases were washed with brine (100 mL), dried over anhydrous sodium sulfate and then concentrated under reduced pressure to give the title compoundThe compound was a light yellow solid (940 mg, 90.86percent). |
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