Method for preparing high-purity docusate sodium
A docusate sodium and esterification technology, which is applied in the field of preparation of high-purity docusate sodium, can solve the problems of inability to obtain purity and high docusate sodium
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Embodiment 1
[0023] In a 500mL three-necked flask equipped with a water separator, a reflux condenser and a thermometer, add 50g (0.5mol) of maleic anhydride, 230mL (1.50mol) of 2-ethylhexanol, and 1.0g of p-toluenesulfonic acid (5mmol), 50mL of toluene, shake well, heat the oil bath to reflux, control the internal temperature at 125-140°C, react for about 1.5hr, separate water 9mL from the water separator (theoretical amount of water generated is 9mL), stop the reaction, cool to light yellow The reaction solution was washed successively with an equal volume of water, 10% NaHCO 3 solution (100ml), and then washed with water (2×100mL), toluene and 2-ethylhexanol were recovered by distillation under reduced pressure to obtain 163.4g of di(2-ethyl)hexyl maleate as light yellow oil, which was collected The rate is 96.0%.
[0024] Di(2-ethyl)hexyl maleate 340g (1.0mol), NaHSO 3 Add 125g (1.2mol) and 300mL of water into a 1000mL autoclave, seal it tightly, and stir and react at 105-110°C for 8...
Embodiment 2
[0027] The reaction operation steps are the same as in Example 1, and the purification steps are as follows: 410g of the crude product of docusate sodium is dissolved in 900mL of absolute ethanol, and there is a small amount of insoluble matter. Add 4 to 5g of activated carbon, filter, and add 90mL of water and 90mL of toluene to the filtrate. After cooling to -5°C, crystals were precipitated, crystallized overnight, and filtered with suction to obtain 348 g of hydrous crystals. The crystals were dissolved in 1500 mL of absolute ethanol, and the ethanol was recovered under reduced pressure to obtain 314 g of powdered docusate sodium, with a sulfonation yield of 70.7% and a purity of 99.5%.
Embodiment 3
[0029]In a 1000mL three-neck flask equipped with a water separator, a reflux condenser and a thermometer, add 50g (0.5mol) of maleic anhydride, 230mL (1.50mol) of 2-ethylhexanol, and 25g001x7 (732) cation exchange Resin and toluene 100mL, shake well, heat the oil bath to reflux, control the internal temperature at 100°C, react for about 3hr, separate out 9mL of water in the water separator (theoretical water volume is 9mL), stop the reaction, cool the light yellow reaction liquid, filter to remove The resin was exchanged, the resin was washed twice with 50 mL of water, the toluene and 2-ethylhexanol were recovered by distillation under reduced pressure, and 163.4 g of di(2-ethyl)hexyl maleate was obtained as light yellow oil, with a yield of 96.0%.
[0030] Di(2-ethyl)hexyl maleate 340g (1.0mol), NaHSO 3 Add 125g (1.2mol) and 300mL of water into a 1000mL autoclave, seal it tightly, and stir and react at 105-110°C for 8 hours to obtain a viscous, colorless and transparent liqui...
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