Method for preparing D-calcium erythorbate
A technology of erythorbic acid and calcium ascorbate, applied in directions such as organic chemistry, can solve problems such as rare application reports of D-calcium ascorbate, no public reports on D-calcium ascorbate synthesis, and achieve stable quality, mild reaction conditions, and technology. Easy to use effect
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Embodiment 1
[0011] At room temperature, 180.0 g of D-erythorbic acid was dissolved in 1200 mL of distilled water, and 46.0 g of light calcium carbonate was slowly added under stirring for neutralization. After the reaction solution turns into a transparent solution, centrifuge (4000r / min, 20min) to remove a very small amount of insoluble impurities. Use a rotary evaporator to concentrate the filtrate under reduced pressure to a syrupy state, add it to 2000 mL of anhydrous methanol, stir slowly for 2 h, and filter to obtain a wet product of calcium D-erythorbate. The wet product of calcium D-erythorbate was dried under reduced pressure for 8 hours to obtain 169.7 g of finished calcium D-erythorbate. The yield is 84.50% of the theoretical yield, and the product purity is 99.31%.
Embodiment 2
[0013] At room temperature, 175.0 g of D-erythorbic acid was dissolved in 1150 mL of distilled water, and 45.0 g of light calcium carbonate was slowly added under stirring for neutralization. After the reaction solution turned into a transparent solution, a small amount of insoluble impurities was removed by suction filtration. Concentrate the filtrate under reduced pressure with a rotary evaporator to a syrupy state, add it to 2000 mL of absolute ethanol, stir slowly for 2.5 h, and filter to obtain a wet product of calcium D-erythorbate. The wet product of calcium D-erythorbate was dried under reduced pressure for 8 hours to obtain 165.4 g of finished calcium D-erythorbate. The yield is 84.17% of the theoretical yield, and the product purity is 98.67%.
Embodiment 3
[0015] At room temperature, 175.0 g of D-erythorbic acid was dissolved in 1150 mL of distilled water, and 27.5 g of calcium oxide was slowly added under stirring for neutralization. After the reaction solution turns into a transparent solution, centrifuge (4000r / min, 20min) to remove a very small amount of insoluble impurities. Concentrate the filtrate under reduced pressure with a rotary evaporator to a syrupy state, add it to 1600 mL of anhydrous methanol, stir slowly for 2 h, and filter to obtain a wet product of calcium D-erythorbate. The wet product of calcium D-erythorbate was dried under reduced pressure for 10 hours to obtain 163.6 g of finished calcium D-erythorbate. The yield is 83.14% of the theoretical yield, and the product purity is 98.54%.
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