Method for synthesizing aromatic aldehyde, aromatic ketone and aromatic ester through catalytically oxidizing alkyl aromatic compound by iron
A technology for aromatic compounds and alkylene oxides, which is applied in the field of catalytic synthesis, can solve the problems of poor compatibility of functional groups, high reaction costs, and low reaction efficiency, and achieve the effects of high selectivity, good reaction selectivity, and wide sources
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Embodiment 1
[0027] Compound 1: Add ferrous acetylacetonate (0.025mmol), polymethylhydrogensiloxane (0.75mmol), potassium persulfate (0.25mmol), 1a (0.25mmol), acetonitrile (1mL), water to a 25mL reaction flask in sequence (1 mL), the reaction mixture was reacted at 80°C for 6h. After the reaction, add ammonia water (2 mL) to remove polymethylhydrogen siloxane, add 10 mL of saturated saline, and extract with ether (10 mL×3), combine the organic phases, evaporate the solvent under reduced pressure, and separate by column chromatography to obtain a yield of 80%. .
Embodiment 2
[0029] Compound 2: Iron acetylacetonate (0.025mmol), polymethylhydrogensiloxane (0.75mmol), potassium persulfate (0.25mmol), 1b (0.25mmol), acetonitrile (1mL), water ( 1 mL), the reaction mixture was reacted at 80°C for 3h. After the reaction, add ammonia water (2 mL) to remove polymethylhydrogen siloxane, add 10 mL of saturated saline, and extract with ether (10 mL×3), combine the organic phases, evaporate the solvent under reduced pressure, and separate by column chromatography to obtain a yield of 80%. .
Embodiment 3
[0031] Compound 3: Add ferrous acetylacetonate (0.025mmol), polymethylhydrogensiloxane (0.75mmol), potassium persulfate (0.25mmol), 1c (0.25mmol), acetonitrile (1mL), water to a 25mL reaction flask in sequence (1 mL), the reaction mixture was reacted at 80° C. for 3 h. After the reaction, add ammonia water (2 mL) to remove polymethylhydrogen siloxane, add 10 mL of saturated saline, and extract with ether (10 mL×3), combine the organic phases, evaporate the solvent under reduced pressure, and separate by column chromatography to obtain a yield of 80%. .
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