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CAS No. : | 29681-43-4 | MDL No. : | MFCD00956223 |
Formula : | C8H9NO3 | Boiling Point : | No data available |
Linear Structure Formula : | - | InChI Key : | OJDKENGKKYVJLY-UHFFFAOYSA-N |
M.W : | 167.16 | Pubchem ID : | 1519345 |
Synonyms : |
|
Signal Word: | Warning | Class: | |
Precautionary Statements: | P261-P305+P351+P338 | UN#: | |
Hazard Statements: | H315-H319-H335 | 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 |
---|---|---|
47% | General procedure: Toa stirred solution of diisopropylamine (1.01mL, 7.18mmol) in dry THF (4 mL) wasadded n-butyllithium in hexane (1.6M in hexanes, (4.48 mL, 7.18 mmol) at -78 Cand stirred for 30 minutes at the same temperature. Methyl 4-methoxypicolinate(0.3g, 1.794mmol) in THF (3 mL) was added to the above solution and stirred forfurther 30 minutes at the same temperature. Disulfide 2a (0.53g, 2.15mmol) in THF (3 mL) was added at - 78oCand the mixture was stirred at the same temperature with continuous monitoringby TLC for 2h. Saturated NH4Cl solution (10 mL) was added to thereaction mixture and slowly warmed to room temperature and extracted with ethylacetate (3x25mL). The combined organic layer was dried over anhydrous Na2SO4and the volatiles were removed under reduced pressure. The resulting crudematerial was purified by column chromatography, eluting with 40% ethyl acetatein hexanes to afford compound 3a aspale yellow solid; Yield: 68%; |
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