Preparation method for citraconic anhydride
A technology of citraconic anhydride and itaconic acid, applied in the direction of organic chemistry, can solve the problems of harsh reaction conditions, high reaction temperature, and many by-products, and achieve the effects of convenient solvent recovery, simple post-treatment, and no impact on yield
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Embodiment 1
[0015] Example 1: 0.10g of strontium sulfate, 10.0g of itaconic acid and 10.0g of tetrahydronaphthalene were added to a reactor equipped with an oil-water separator, a thermometer and agitation, and the reaction was stopped after water separation at 210°C for 4 hours, and the resulting product was decompressed Distillation, under a vacuum of 300Pa, distill the solvent at 85°C to recover the solvent, and collect the product at 100°C to obtain a colorless liquid product, citraconic anhydride, with a yield of 99.0% and a purity of 99.6%.
Embodiment 2
[0019] Embodiment 2: 0.10g magnesium sulfate, 50.0g itaconic acid and 500.0g o-dichlorobenzene are added in the reactor that is equipped with oil-water separator, thermometer and stirring, stop reaction after 10h of water separation reaction at 155 ℃, the gained product is reduced Pressure distillation, under vacuum degree of 300Pa, distill and recover the solvent at 85°C, and collect the product at 100°C to obtain a colorless liquid product, citraconic anhydride, with a yield of 98.2% and a purity of 99.3%.
Embodiment 3
[0020] Example 3: 1.0g of barium sulfate, 50.0g of itaconic acid and 10.0g of xylene were added to a reactor equipped with an oil-water separator, a thermometer and agitation, and the reaction was stopped after 1.0h of water separation at 130°C, and the resulting product was decompressed Distillation, under a vacuum of 300Pa, distill the solvent at 85°C to recover the solvent, and collect the product at 100°C to obtain a colorless liquid product, citraconic anhydride, with a yield of 97.5% and a purity of 99.5%.
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