Method for preparing 2, 4-dihydroxy benaophenonel by using aluminum trichloride to catalyze
A technology of dihydroxybenzophenone and aluminum trichloride, applied in the direction of condensation preparation of carbonyl compounds, organic chemistry, etc., can solve the problems of industrial waste pollution, low product yield, complex decolorization and purification process, etc., and achieve easy Separation and purification, good color effect
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specific Embodiment 1
[0016] Prepare 2,4-dihydroxybenzophenone as follows:
[0017] (a) Weigh resorcinol, benzoyl chloride, aluminum trichloride and chlorobenzene in a ratio of 1:1:2:2;
[0018] (b) Put the raw materials weighed in step (a) into the reaction container at the same time, heat and stir until each component is fully dissolved, and react at 50-70°C for 5-6 hours;
[0019] (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.
[0020] The product yield of gained 2,4-dihydroxybenzophenone is 60%.
specific Embodiment 2
[0021] Prepare 2,4-dihydroxybenzophenone as follows:
[0022] (a) Weigh resorcinol, benzoyl chloride, aluminum trichloride and chlorobenzene in a substance ratio of 1:2:2:4;
[0023] (b) Put the raw materials weighed in step (a) into the reaction container at the same time, heat and stir until each component is fully dissolved, and react at 50-70°C for 5-6 hours;
[0024] (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.
[0025] The product yield of gained 2,4-dihydroxybenzophenone is 70%.
specific Embodiment 3
[0026] Prepare 2,4-dihydroxybenzophenone as follows:
[0027] (a) Weigh resorcinol, benzoyl chloride, aluminum trichloride and chlorobenzene in a substance ratio of 1:2:2:4;
[0028] (b) Put in benzoyl chloride, aluminum trichloride and chlorobenzene and heat and stir until they are fully dissolved, then slowly add resorcinol dropwise while heating and stirring to react, and react at 50-70°C for 3-4 hours;
[0029] (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.
[0030] The product yield of gained 2,4-dihydroxybenzophenone is 75%.
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