Method for preparing 2, 4-dihydroxy benaophenonel by using indium trichloride to catalyze
A technology of dihydroxybenzophenone and indium trichloride is applied in the field of catalyzing the preparation of 2,4-dihydroxybenzophenone by indium trichloride, which can solve industrial waste pollution, high production energy consumption and product yield. problems such as low rate, to achieve the effect of easy separation and purification, and damage reduction
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specific Embodiment 1
[0017] Prepare 2,4-dihydroxybenzophenone as follows:
[0018] (a) Put resorcinol, benzoic acid, indium trichloride, and water into the reaction vessel in a ratio of 10:10:1:100;
[0019] (b) Heat to 105-110°C, stir until the components in step (a) are fully dissolved, and reflux for 3-5 hours;
[0020] (c) After the reaction is completed, pour the reaction solution in step (b) into cold water, crystallize, filter, and dry to obtain 2,4-dihydroxybenzophenone.
[0021] The product yield of gained 2,4-dihydroxybenzophenone is 80%.
specific Embodiment 2
[0022] Prepare 2,4-dihydroxybenzophenone as follows:
[0023] (a) Put resorcinol, benzoic acid, indium trichloride, and water into the reaction vessel in a ratio of 10:20:3:150;
[0024] (b) Heat to 105-110°C, stir until the components in step (a) are fully dissolved, and reflux for 3-5 hours;
[0025] (c) After the reaction is completed, pour the reaction solution in step (b) into cold water, crystallize, filter, and dry to obtain 2,4-dihydroxybenzophenone.
[0026] The product yield of gained 2,4-dihydroxybenzophenone is 85%.
specific Embodiment 3
[0027] Prepare 2,4-dihydroxybenzophenone as follows:
[0028] (a) Put resorcinol, benzoic acid, indium trichloride, and n-hexane into the reaction vessel at a ratio of 10:20:3:150;
[0029] (b) Heat to 70-75°C, stir until the components in step (a) are fully dissolved, and reflux for 6-8 hours;
[0030] (c) After the reaction is completed, pour the reaction solution in step (b) into cold water, crystallize, filter, and dry to obtain 2,4-dihydroxybenzophenone.
[0031] The product yield of gained 2,4-dihydroxybenzophenone is 70%. This shows that the reaction time required for normal hexane as a solvent is longer, and the product yield is not as high as water as a solvent.
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