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CAS No. : | 38202-27-6 | MDL No. : | MFCD00009244 |
Formula : | C13H19NO4S | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | - |
M.W : | 285.36 | Pubchem ID : | - |
Synonyms : |
|
Signal Word: | Danger | Class: | 4.1 |
Precautionary Statements: | P240-P210-P241-P264-P280-P302+P352-P370+P378-P337+P313-P305+P351+P338-P362+P364-P332+P313 | UN#: | 1325 |
Hazard Statements: | H315-H319-H228 | Packing Group: | Ⅱ |
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 |
---|---|---|
2.73 g | Stage #1: With perchloric acid In tetrahydrofuran at 0℃; for 1.5 h; Stage #2: at 0 - 35℃; Stage #3: With potassium carbonate In N,N-dimethyl-formamide at 10 - 35℃; |
To a solution of ethyl N-(mesitylsulfonyl)oxyacetoimidate (14.7 g) in THF (15 mL) was added 60percent perchloric acid (11.2 mL) at 0°, the mixture was stirred for 90 min, and to the reaction mixture was added ice water. The insoluble substance was collected by filtration, washed with water, and dried under stream. The residue was added to a solution of 4-methylpyridine (4.18 mL) in THF (80 mL) at 0° C., and the mixture was stirred overnight at room temperature. The solvent was evaporated under reduced pressure, DMF (80 mL), ethyl propionate (5.21 mL) and potassium carbonate (11.9 g) were added thereto, and the mixture was stirred overnight at room temperature. To the reaction mixture was added water, and the mixture was extracted with ethyl acetate. The extract was washed with 1N hydrochloric acid and saturated brine, and dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (2.73 g). 1H NMR (300 MHz, CDCl3) δ 1.41 (3H, t, J=7.2 Hz), 2.47 (3H, s), 4.38 (2H, q, J=6.9 Hz), 6.77 (1H, dd, J=7.0, 1.7 Hz), 7.93 (1H, s), 8.34 (1H, s), 8.39 (1H, d, J=7.2 Hz). |
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