Method for synthesizing carboxylic acid or ketone compounds from alcohol or aldehyde by taking oxygen or oxygen in air as oxidant
A technology of ketone compounds and oxidants, which is applied in the direction of oxidative preparation of carbonyl compounds, preparation of organic compounds, organic chemical methods, etc., can solve the problem of low catalytic activity, and achieve the effects of environmental friendliness, high yield and mild reaction conditions
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Embodiment 1
[0031]
[0032] Add ferric nitrate nonahydrate (401.8mg, 1.0mmol), 4-hydroxy-2,2,6,6-tetramethylpiperidine oxide (172.4mg, 1.0mmol), potassium chloride (75.9mg , 1.0mmol), 1a (1.4381g, 10.0mmol) and 1,2-dichloroethane (2mL), pumped gas (pure oxygen) three times, stirred at room temperature (25°C) for 33 hours, and obtained 49% 2a (with dibromomethane as internal standard, NMR yield), 39% of 3a (with dibromomethane as internal standard, NMR yield).
Embodiment 2
[0034]
[0035] Add ferric nitrate nonahydrate (405.8mg, 1.0mmol), 4-hydroxy-2,2,6,6-tetramethylpiperidine oxide (171.4mg, 1.0mmol), potassium chloride (75.7mg , 1.0mmol), 1a (1.4353g, 10.0mmol) and dichloromethane (2mL), exchanged gas (pure oxygen) three times, and stirred at room temperature (25°C) for 33 hours to obtain 41% of 2a (based on dibromomethane Internal standard, NMR yield), 27% of 3a (with dibromomethane as internal standard, NMR yield).
Embodiment 3
[0037]
[0038] Add ferric nitrate nonahydrate (403.5mg, 1.0mmol), 4-hydroxy-2,2,6,6-tetramethylpiperidine oxide (171.6mg, 1.0mmol), potassium chloride (75.0mg , 1.0mmol), 1a (1.4359g, 10.0mmol) and toluene (2mL), gas exchanged (pure oxygen) three times, and stirred at room temperature (25°C) for 24 hours to obtain 25% of 2a (with dibromomethane as internal standard , NMR yield), 63% of 3a (with dibromomethane as internal standard, NMR yield).
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