A kind of hydrolysis method of astilbin
A technology of astilbin and hydrolyzate, which is applied in the field of natural medicinal chemistry, can solve the problems of increased production cost, pollution, waste of resources and the environment, and achieve the effects of reducing waste of resources and environmental pollution, facilitating industrial production, and reducing production costs
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0035] The hydrolysis method of astilbin in this embodiment includes the following steps of hydrolyzing astilbin to prepare taxifolin:
[0036] (1) Take 50 g of astilbin, add 350 mL of 2.5 mol / L citric acid aqueous solution under stirring, and hydrolyze at 90°C for 3.5 hours to obtain a hydrolyzate;
[0037] (2) Filtrate the hydrolyzate while it is hot, concentrate the filtrate to 200mL, let it stand for at least 12h, crystallize, filter, collect the filter cake and filtrate respectively, and the filter cake is the crude taxifolin;
[0038] (3) The crude taxifolin is recrystallized, and the specific conditions for recrystallization are as follows: the crude taxifolin is dissolved in water at 40° C., and then cooled to room temperature to obtain taxifolin.
[0039] The hydrolysis method of astilbin in this embodiment also includes the following step of hydrolyzing astilbin to prepare rhamnose: the above filtrate is purified by AB-8 macroporous resin column chromatography, using...
Embodiment 2
[0042] The hydrolysis method of astilbin in this embodiment includes the following steps of hydrolyzing astilbin to prepare taxifolin: (1) take 50 g of astilbin, add 500 mL of 1.5 mol / L citric acid aqueous solution under stirring, and hydrolyze at 105°C for 3 hours, get hydrolyzate;
[0043] (2) Filtrate the hydrolyzate while it is hot, concentrate the filtrate to 190mL, let it stand for at least 12h, crystallize, filter, collect the filter cake and filtrate respectively, and the filter cake is the crude taxifolin;
[0044] (3) The crude taxifolin is recrystallized, and the specific conditions for recrystallization are as follows: the crude taxifolin is dissolved in water at 80° C., and then cooled to room temperature to obtain taxifolin.
[0045] The above filtrate was purified by AB-8 macroporous resin column chromatography, using water as the eluent, collecting the eluate, concentrating until the Brix ratio was 54-56%, standing at 4°C for crystallization to obtain rhamnose....
Embodiment 3
[0049] The hydrolysis method of astilbin in this embodiment includes the following steps of hydrolyzing astilbin to prepare taxifolin:
[0050] (1) Take 50 g of astilbin, add 750 mL of 1.0 mol / L citric acid aqueous solution under stirring, and hydrolyze at 115 ° C for 2 hours to obtain a hydrolyzate;
[0051] (2) Filtrate the hydrolyzate while it is hot, concentrate the filtrate to 210mL, let it stand for at least 12h, crystallize, filter, collect the filter cake and filtrate respectively, and the filter cake is the crude taxifolin;
[0052] (3) The crude taxifolin is recrystallized, and the specific conditions for recrystallization are as follows: the crude taxifolin is dissolved in water at 60° C., and then cooled to room temperature to obtain taxifolin.
[0053] The hydrolysis method of astilbin in this embodiment also includes the following step of hydrolyzing astilbin to prepare rhamnose: the above filtrate is purified by AB-8 macroporous resin column chromatography, usin...
PUM
Login to View More Abstract
Description
Claims
Application Information
Login to View More 
