Hydrolysis method for pleuromutilin
A technology for pleuromutilin and hydrolyzate, which is applied in chemical instruments and methods, preparation of organic compounds, carbon-based compounds, etc., can solve the problems of large environmental pollution and complex product processing, and achieve high product yield and production The effect of short cycle and reduced usage
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Embodiment 1
[0020] Slowly add 2 times the volume of sulfuric acid aqueous solution with a concentration of 1mol / L to the pleuromutilin butyl acetate extract with a mass volume concentration of 10%, and raise the temperature to 80°C for 6 hours under stirring; after the reaction is completed, let it stand Separate the layers, discard the water phase, concentrate the upper butyl acetate phase in vacuum at 65°C, add hot water 0.5 times the volume of the concentrated solution, and wash twice. After washing, add anhydrous sodium sulfate to dehydrate, and filter; The temperature of the solution was slowly lowered to 0°C, the product was precipitated, filtered and dried to obtain the hydrolyzed product of pleuromutilin. Yield 94%, purity 92.4%.
Embodiment 2
[0022] Slowly add 2 times its volume, 1.5 mol / L sulfuric acid aqueous solution to the 12% pleuromutilin butyl acetate extract, stir and raise the temperature to 90°C for 6 hours; layer, discard the water phase, concentrate the upper butyl acetate phase in vacuum at 70°C, add hot water 1 times the volume of the concentrated solution to wash 3 times, add anhydrous sodium sulfate to dehydrate, and filter; the filtrate Slowly lower the temperature to 0°C, the product precipitates, and is filtered and dried to obtain pleuromutilin hydrolyzate. Yield 90%, purity 93.7%.
Embodiment 3
[0024] Slowly add 3 times its volume, 2mol / L sulfuric acid aqueous solution to the pleuromutilin butyl acetate extract with a mass volume concentration of 15%, and heat up to 80°C for 5 hours under stirring; after the reaction is completed, let stand and separate , discard the water phase, vacuum concentrate the upper butyl acetate phase at 70°C, add hot water 1 times the volume of the concentrated solution to wash 3 times, add anhydrous calcium chloride for dehydration after washing, and filter; the filtrate Slowly lower the temperature to 5°C, the product precipitates, and is filtered and dried to obtain the pleuromutilin hydrolyzate. Yield 89%, purity 95.6%.
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