Method for producing L-ascorbyl palmitate through non-aqueous phase enzymatic synthesis
A technology of ascorbyl palmitate and enzymatic synthesis, applied in directions such as fermentation, can solve the problems of unfavorable environment and low yield of waste liquid discharge, and achieve the effects of facilitating large-scale production, high yield and improving yield
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example 1
[0032] Add 10Kg of L-ascorbic acid, 30Kg of palmitic acid, and 350L of tert-butanol into the reaction kettle, add immobilized lipase Novozyme435, and catalyze the reaction for 40 hours at a temperature of 55°C and a stirring speed of 120rpm. The obtained reaction liquid is recovered by suction filtration to recover the immobilized lipase and undissolved L-ascorbic acid, and the resulting filtrate was evaporated under reduced pressure at 55°C to remove the solvent tert-butanol. The residue was dissolved in 400L ethyl acetate, washed twice with deionized water, the ethyl acetate phase was separated, and the ethyl acetate solvent was evaporated under reduced pressure at 50°C to obtain a crude product. The crude product was dissolved by heating with 400L toluene at 60°C, cooled and crystallized at room temperature, centrifuged to obtain a filter cake, washed twice with n-hexane, centrifuged at 50°C, and vacuum-dried at -0.09MPa for 2 hours to obtain the target product L-ascorbyl pa...
example 2
[0034]Add 10Kg of L-ascorbic acid, 24Kg of palmitic acid, and 380L of tert-butanol into the reaction kettle, add immobilized lipase Novozyme435, and catalyze the reaction at a temperature of 50°C and a stirring speed of 120rpm for 36 hours. The obtained reaction solution is suction filtered to remove the immobilized lipase and undissolved L-ascorbic acid, the resulting filtrate was evaporated under reduced pressure at 55°C to remove the solvent tert-butanol, the residue was dissolved in 350L ethyl acetate, washed twice with deionized water, the ethyl acetate phase was separated, and then reduced to 50°C The solvent ethyl acetate was removed by evaporation under reduced pressure to give crude product. The crude product was dissolved by heating with 350L toluene at 60°C, cooled and crystallized at room temperature, centrifuged to obtain a filter cake, washed twice with n-hexane, centrifuged at 50°C, and vacuum-dried at -0.09MPa for 2 hours to obtain the target product L-ascorbyl ...
example 3
[0036] Add 10Kg of L-ascorbic acid, 32Kg of palmitic acid, and 350L of tert-butanol into the reaction kettle, add the immobilized lipase Lipozyme TLIM, and catalyze the reaction at a temperature of 55°C and a stirring speed of 120rpm for 40 hours. The obtained reaction solution is suction filtered to remove the immobilized fat Enzyme and undissolved L-ascorbic acid, the resulting filtrate was evaporated under reduced pressure at 58°C to remove the solvent tert-butanol, the residue was dissolved in 300L ethyl acetate, washed twice with deionized water, the ethyl acetate phase was separated, and then heated at 50°C The solvent ethyl acetate was evaporated under reduced pressure to obtain a crude product. The crude product was dissolved by heating with 200L toluene at 60°C, cooled and crystallized at room temperature, centrifuged to obtain a filter cake, washed twice with n-hexane, centrifuged at 52°C, and vacuum-dried at -0.09MPa for 2 hours to obtain the target product L-ascorby...
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