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CAS No. : | 226888-37-5 | MDL No. : | MFCD09909451 |
Formula : | C9H8FNO4 | Boiling Point : | No data available |
Linear Structure Formula : | - | InChI Key : | XRTVFSTWEJOKNN-UHFFFAOYSA-N |
M.W : | 213.16 | Pubchem ID : | 22742120 |
Synonyms : |
|
Signal Word: | Warning | Class: | |
Precautionary Statements: | P261-P305+P351+P338 | UN#: | |
Hazard Statements: | H302-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 |
---|---|---|
97% | at 80℃; | A mixture of 2-(4-fluoro-3-nitrophenyl)acetic acid (28.8 g, 0.14 mmol) and cone. H2S04 (10 ml_) in MeOH (30 ml_) was stirred at 80°C overnight. The resulting mixture was quenched with ice water and extracted with EtOAc. The organic layer was washed with sat. NaHC03 aq. solution and brine, dried over Na2S04, filtered and concentrated to give the title compound (30 g, 97percent yield) as a yellow oil. LCMS (ESI) m/z calcd for C9H8FN04: 213.04. Found: 214.26 (M+1)+. |
87% | for 2 h; | 4-fluoro-3-nitrophenylacetic acid (4. 55g, 22.9 MMOL) was suspended in 50 ml MEOH and added 0.15 mi H2SO4 followed by reflux for 2h. After cooling the reaction mixture was poured into water and then added NAHCO3 until PH>7. The extraction with EtOAc, drying with MGS04 and evaporation in vacuo gave 5e. Yield 4. 259, 87percent. |
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