Method for preparing aromatic ketone or aromatic aldehyde by selectively oxidizing alkyl arene
A technology for aromatic ketones and aromatic aldehydes, applied in the field of selective oxidation of alkyl aromatics to aromatic ketones or aromatic aldehydes, can solve the problems of poor product selectivity, poor atom economy, high reaction temperature, etc., and achieve low cost and high selectivity , the effect of meeting the requirements of technical economy
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Embodiment 1
[0018] Example 1: Catalytic oxidation of indane
[0019] Dissolve 1ml (8.1mmol) of indane in 10ml of acetonitrile, add 0.20mmol of acriflavine, 0.24mmol of molecular bromine and 0.67mmol of N-hydroxyphthalimide, at 75°C, 0.3MPa of O 2 Under pressure, after reacting for 5 hours, analyze the reaction result with a gas chromatograph; the conversion rate of indane can reach 92%, and the selectivity of indan-1-one can reach 79%; at this time, it can be cooled, distilled, and the product can be collected.
Embodiment 2
[0020] Example 2: Catalytic oxidation of indane
[0021] Dissolve 1ml (8.1mmol) of indane in 10ml of methanol, add 0.01mmol of acriflavine, 0.08mmol of molecular bromine and 0.67mmol of N-hydroxyphthalimide, at 50°C, 0.3MPa of O 2 Under pressure, after reacting for 25 hours, analyze the reaction result with a gas chromatograph; the conversion rate of indan can reach 73%, and the selectivity of indan-1-one can reach 54%; at this time, it can be cooled and distilled to collect the product.
Embodiment 3
[0022] Example 3: Catalytic oxidation of indane
[0023] Dissolve 1ml (8.1mmol) indane in 10ml ethyl acetate, add 0.20mmol acridine, 0.24mmol molecular bromine and 0.08mmol N-hydroxyphthalimide, at 200°C, 0.001MPa O 2 Under pressure, after reacting for 5 hours, analyze the reaction result with a gas chromatograph; the conversion rate of indane can reach 19%, and the selectivity of indan-1-one can reach 13%; at this time, it can be cooled, distilled, and the product can be collected.
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