Method for synthesizing EGCG fatty acid ester catalyzed by immobilized enzyme
A technology for immobilizing lipase and fatty acid ester, applied in the field of enzyme catalysis, can solve problems such as the difficulty of EGCG phenolic hydroxyl reaction, and achieve the effects of being conducive to continuous production, increasing solubility, and simple separation and purification
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Embodiment 1
[0029] Take EGCG monomer 1.00g (2.18mmol), vinyl acetate 0.188g (2.18mmol), dissolve in 10ml ethyl acetate, add immobilized lipase 0.5g, under the condition of temperature 30 ℃, in the shaker (180r / min), reacted for 120 hours, and the EGCG conversion rate was 20%; the immobilized lipase was taken out, and the reaction solution was filtered, concentrated under reduced pressure, and desolvated to obtain 0.24 g of tan powdery EGCG acetate.
Embodiment 2
[0031]Take EGCG monomer 1.00g (2.18mmol), vinyl acetate 0.188g (2.18mmol), dissolve in 10ml ethyl acetate, add immobilized lipase 1g, under the condition of temperature 40 ℃, in the shaker (180r / min), reacted for about 120 hours, and the EGCG conversion rate was 25%; the immobilized lipase was taken out, and the reaction solution was filtered, concentrated under reduced pressure, and desolventized to obtain 0.30 g of tan powdery EGCG acetate.
Embodiment 3
[0033] Take EGCG monomer 1.00g (2.18mmol), vinyl acetate 0.188g (2.18mmol), dissolve in 10ml tetrahydrofuran, add immobilized lipase 2.0g, under the condition of temperature 40 ℃, in the shaker (180r / min ), reacted for 120 hours, and the EGCG conversion rate was 30%; the immobilized lipase was taken out, and the reaction solution was filtered, concentrated under reduced pressure, and desolvated to obtain 0.35 g of tan powdery EGCG acetate.
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