Alkylbenzene photooxidizing process with oxygen to prepare aromatic aldehyde and aromatic acid
A technology for photo-oxidation of alkylbenzenes and aromatic aldehydes, which can be used in chemical instruments and methods, preparation of carbon-based compounds, preparation of organic compounds, etc., and can solve problems such as environmental pollution
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Embodiment 1
[0023] Dissolve 2,4,6-triphenylpyranyl boron tetrafluoride and toluene in a glass reactor filled with dichloromethane at a molar ratio of 1:10, stir and fill at an oxygen pressure lower than three Oxygen for 20 minutes, and then react with a 100-watt mercury lamp (light <310 nm is filtered out). Oxygen was charged after every 4 hours of reaction. After reacting at room temperature for 10 hours, the reaction is terminated, and as a result, the total yield of benzaldehyde and benzoic acid can reach more than 90%.
Embodiment 2
[0025] Dissolve 2,4,6-triphenylpyranyl boron tetrafluoride and p-xylene at a molar ratio of 1:20 in a glass reactor filled with dichloromethane. Stir and oxygenate for 15 minutes, and then react under irradiation with a 100-watt mercury lamp (light <310nm is filtered out). Oxygen was charged after every 2 hours of reaction. After reacting at room temperature for 5 hours, the reaction is terminated, and as a result, the total yield of p-benzaldehyde and p-benzoic acid can reach more than 95%.
Embodiment 3
[0027] Dissolve 2-p-methoxy-4,6-diphenylpyranyl boron tetrafluoride and p-xylene at a molar ratio of 1:10 in a glass reactor filled with dichloromethane. Stir and oxygenate for 20 minutes under an oxygen pressure of 1 atmosphere, and then react under irradiation with a 500-watt tungsten lamp (the light of <420nm is filtered out). Oxygen was charged after every 4 hours of reaction. After reacting at room temperature for 10 hours, the reaction is terminated, and as a result, the total yield of p-tolualdehyde and p-toluic acid can reach more than 72%.
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