Catalyst and preparation method for synthesizing salicylic acid by carboxylation reaction of phenol
A technology of phenol carboxyl group and catalyst, which is applied in the field of catalyst and preparation of phenol carboxylation reaction to synthesize salicylic acid, can solve the problems of harsh reaction conditions, high reaction efficiency, low reaction activity, etc., and achieve simple recycling, high catalytic activity, Strong solubility effect
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Embodiment 1
[0029] Preparation of [Bmim]Br / AlBr 3 : Step 1 {[Bmim]Br}: Weigh 64.12g (0.78mol) of 1-methylimidazole into a 500ml three-necked flask, and stir rapidly at a constant temperature of 70°C. Slowly add 117.87 g (0.858 mol) of n-bromobutane dropwise into the three-necked flask with a constant pressure dropping funnel for 1 h. After the dropwise addition, the mixture was refluxed at 70° C. for 10 h. After the reaction was completed, cool to room temperature to obtain the crude product [Bmim]Br, which was transferred to a separatory funnel, washed (3 times) with 30ml ethyl acetate, and then the product was rotary evaporated at 60°C for 30min to remove residual ethyl acetate. ester. The remaining product was transferred to a beaker and placed in a vacuum drying oven at a temperature of 65°C, and dried to constant weight to obtain the finished product of 1-methyl-3-n-butylimidazole bromide ([Bmim]Br). Step 2 {[Bmim]Br / AlBr 3}: Weigh 50g of prepared [bmim]Br into a 250ml single-nec...
Embodiment 2
[0031] Preparation of Fe 3 o 4 @Zn-ZIF-8: Weigh 1.77g of zinc nitrate hexahydrate and dissolve it in 60.5ml of anhydrous methanol to obtain solution 1; weigh 9.85g of 2-methylimidazole and dissolve it in 60.5ml of anhydrous methanol to obtain a solution 2; After mixing solution 1 with solution 2, add 0.08g Fe 3 o 4 Disperse into the mixed liquid, stir magnetically at 50°C for 4h; after the reaction, centrifuge at 8000r.p.m, and wash with methanol three times; the obtained solid is vacuum-dried at 80°C overnight, and ground to obtain Fe3O4@Zn-ZIF-8 . like figure 2 Shown is Fe3O4@Zn-ZIF-8 obtained in the present invention. Example 3
Embodiment 3
[0032] Preparation of [Bmim]Br / AlBr3-Fe 3 o 4 @Zn-ZIF-8: Dissolve 0.4g of ionic liquid [Bmim]Br / AlBr3 in 5ml of anhydrous methanol, and weigh 0.63g of Fe 3 o 4 @ZIF-8 added [Bmim]Br / AlBr 3 After ultrasonic treatment for 10 minutes, seal it with plastic wrap and place it in a ventilated place for immersion for 24 hours, then separate the catalyst with a magnet, dry it in a vacuum oven at 80°C overnight, and place the solid catalyst in a muffle furnace for calcination at 220°C After grinding, the recyclable MOFs immobilized ionic liquid catalyst [Bmim]Br / AlBr3-Fe3O4@Zn-ZIF-8 was obtained. like image 3 Shown is [Bmim]Br / AlBr3-Fe3O4@Zn-ZIF-8 obtained in the present invention.
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