Method for preparing p-benzoquinone compound by dual catalytic system
A technology of phenol compound and p-benzoquinone, which is applied in the preparation field of oxidative synthesis of p-benzoquinone compound under a dual catalyst system, can solve the problems of large amount of transition metal catalyst, non-recyclable catalyst, and affecting the economic benefits of mass production of products, etc. Achieve the effect of green production process, good catalytic activity and stability, and save production cost
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Embodiment 1
[0024] 94g of phenol, 0.94g of copper nitrate, 4.7g of 1-sulfopropyl-2-hydroxymethyl 3-methylimidazolium tetrafluoroborate ionic liquid, and 100ml of methanol were successively added to the 1L reactor equipped with an oil bath heating device, After the reactor was closed, 50 atm of oxygen was introduced and kept at constant pressure, heated to 90°C, stirred and reacted for 2.5 hours and then cooled to room temperature naturally. After exhausting, the catalyst was separated from the reaction system, and the reaction mixture was analyzed to obtain p-benzoquinone: 15.7g .
Embodiment 2
[0026] 94g of phenol, 0.94g of copper nitrate, 4.7g of 1-sulfopropyl-2-hydroxymethyl 3-methylimidazolium tetrafluoroborate ionic liquid, and 100ml of methanol were successively added to the 1L reactor equipped with an oil bath heating device, After the reactor was closed, 40 atm of oxygen was introduced and kept at constant pressure, heated to 80°C, stirred and reacted for 1.5 hours and then cooled to room temperature naturally. After exhausting the catalyst, the catalyst was separated from the reaction system, and the reaction mixture was analyzed to obtain p-benzoquinone: 35.9g .
Embodiment 3
[0028] 60g of phenol, 1.2g of manganese nitrate, 3.6g of 1-sulfopropyl-2-hydroxymethyl 3-methylimidazolium tetrafluoroborate ionic liquid and 100ml of methanol were successively added to the 1L reactor equipped with an oil bath heating device, After the reactor was closed, 30 atm of oxygen was introduced and kept at constant pressure, heated to 70°C, stirred and reacted for 2 hours and then cooled to room temperature naturally.
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