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CAS No. : | 4142-98-7 | MDL No. : | MFCD00020122 |
Formula : | C9H10O4 | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | APHYVLPIZUVDTK-UHFFFAOYSA-N |
M.W : | 182.17 | Pubchem ID : | 20098 |
Synonyms : |
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Signal Word: | Warning | Class: | N/A |
Precautionary Statements: | P261-P305+P351+P338 | UN#: | N/A |
Hazard Statements: | H302-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 |
---|---|---|
15.1% | With sodium formate;palladium on activated charcoal; In ethanol; at 30 - 40℃; for 3.0h; | Reference Example 3 Synthesis of ethyl 3-hydroxy-5-oxo-cyclohexa-3-ene carboxylate To an ethanol solution (200 mL) of 3,5-dihydroxybenzoic acid (25 g, 162.2 mmol) was added sulfuric acid (3 mL) and stirred over night at room temperature and then under heating at 65C for 4 days. The reaction liquid was concentrated under reduced pressure and poured into ice water (about 300 mL) while stirring to filter off white crystal, 3,5-dihydroxybenzoic acid ethyl ester (22.8 g, 77.2%). 3,5-Dihydroxybenzoic acid ethyl ester (10 g, 54.89 mmol) was dissolved in ethanol (15 mL), followed by adding sodium formate (4.48 g, 65.87 mmol), replacing inside a reactor with nitrogen at 30C for 15 minutes, adding palladium on carbon (364 mg) and reacting at 30C for 3 hours then at 40C over night. Catalyst was filtered off, followed by neutralization with a 1N HCl solution, concentration under reduced pressure and purification of thus obtained residue with silica gel column chromatography (hexane/ethyl acetate=1/1 to 0/1) to obtain an objective compound (1.53 g, 15.1%). 1H-NMR (200 MHzFT,TMS,CDCl3) 1.26(3H,dt,J=1.8,7.1Hz), 2.66(2H,d,J=2.7Hz), 2.83(1H,dd,J=1.8,6.6Hz), 3.01-3.19(1H,m), 3.32-3.55(1H,m), 4.18(2H,q,J=7.2Hz), 5.51(1H,s), 5.80-6.10(1H,br) MS(ESI) m/z 185 [M+H]+ |
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