Method for synthesizing 6''-O-lauroyl-naringin ester on line by using lipase as catalyst

A lipase and lauroyl technology, which is applied in the field of lipase-catalyzed online controllable and selective synthesis of 6''-O-lauroyl-naringin ester, can solve the problem of low conversion rate and selectivity, long reaction time, etc. problems, to achieve the effect of shortening the reaction time, high reaction selectivity, and high conversion rate

Active Publication Date: 2014-03-26
ZHEJIANG UNIV OF TECH
View PDF1 Cites 12 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0008] At present, many domestic and foreign scholars have studied the enzyme-catalyzed synthesis of naringin esters in organic media, but this method often requires a long reaction time (24h), and the conversion rate ...

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Method for synthesizing 6''-O-lauroyl-naringin ester on line by using lipase as catalyst
  • Method for synthesizing 6''-O-lauroyl-naringin ester on line by using lipase as catalyst
  • Method for synthesizing 6''-O-lauroyl-naringin ester on line by using lipase as catalyst

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0032] Example 1: Synthesis of 6''-O-lauroyl-naringin ester

[0033]

[0034] Device reference used figure 1 . Dissolve naringin (0.49mmol) in 10mL of tert-amyl alcohol:DMSO=4:1 (v / v) mixed solvent, vinyl laurate (3.43mmol) in 10mL of tert-amyl alcohol, and then put them in Ready-to-use in a 10mL syringe. 0.87g of lipase Lipozyme RMIM was evenly filled in the reaction channel of the microfluidic channel reactor, driven by the PHD2000 syringe pump, the two reaction solutions were divided into a total of 10.4 μL min -1 The flow rate of the flow rate enters the reaction channel through the "Y" joint for reaction, and the temperature of the reactor is controlled at 52°C through a water bath thermostat. The flow reaction was carried out for 30 minutes, and the reaction result was tracked and detected by thin-layer chromatography (TLC).

[0035] The reaction solution was collected online through the product collector, the solvent was distilled off under reduced pressure, and ...

Embodiment 2-5

[0041] Change the temperature of the microfluidic channel reactor, others are the same as in Example 1, and the reaction results are as shown in Table 1:

[0042] Table 1: Effect of Temperature on Reaction

[0043]

[0044] The results in Table 1 show that when the flow rate is 10.4 μL min -1 , when the reaction time is 30min, the conversion rate increases obviously with the increase of the reaction temperature. When the reaction temperature reaches 52°C, the conversion rate and selectivity of the reaction are the best. The decrease in enzyme activity leads to a decrease in the conversion rate and selectivity of the reaction, so the optimal reaction temperature of naringin laurate in the microfluidic microchannel reactor in the present invention is 52°C.

Embodiment 6-9

[0046] Change the substrate molar ratio of vinyl laurate to naringin in the microfluidic microchannel reactor to 1:1 (Example 6), 3:1 (Example 7), 5:1 (Example 8), 9:1 ​​(Example 9), the dosage of naringin was 0.49mmol unchanged, and the dosage of vinyl laurate was changed. Others are the same as Example 1, and the results are shown in Table 2.

[0047] Table 2: Effect of Naringin and Vinyl Laurate Substrate Ratio on Reaction

[0048]

[0049] The result of table 2 shows, along with the increase of reactant vinyl laurate, the conversion rate of reaction also increases thereupon, and when substrate ratio is 7:1, the conversion rate and selectivity of reaction are optimal, and naringin basically There has been quantitative complete conversion to naringin-6''-laurate. Now if continue to increase the consumption of reactant vinyl laurate, will cause the conversion rate of reaction and selectivity to reduce, thereby, the optimum substrate ratio of this reaction is 7:1, under t...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

PUM

No PUM Login to view more

Abstract

The invention discloses a method for synthesizing a 6''-O-lauroyl-naringin ester on line by using lipase as a catalyst, which comprises the following steps: by using naringin and vinyl laurate in a mole ratio of 1:(1-9) as raw materials, 0.5-1.0g of lipase Lipozyme RMIM as a catalyst and a tertiary amyl alcohol-DMSO (dimethyl sulfoxide) mixed solvent as a reaction solvent, uniformly filling the lipase Lipozyme RMIM into a reaction channel of a microfluidic channel reactor, wherein the internal diameter of the reaction channel of the microfluidic channel reactor is 0.8-2.4mm, and the reaction channel is 0.5-1.0m long; continuously introducing the raw materials and the reaction solvent into the reaction channel to perform acylation reaction, wherein the acylation reaction temperature is controlled at 40-55 DEG C, and the acylation reaction time is 15-35 minutes; and collecting the reaction solution on line, and carrying out conventional after-treatment on the reaction solution to obtain the 6''-O-lauroyl-naringin ester. The method has the advantages of short reaction time, high selectivity and high yield.

Description

(1) Technical field [0001] The invention relates to a lipase-catalyzed online controllable selective synthesis method of 6''-O-lauroyl-naringin ester. (2) Background technology [0002] Naringin (Naringin), also known as naringin, citrusin, isohesperidin, is a dihydroflavonoid compound, mainly found in the peel and pulp of pomelo fruit, grapefruit, tangerine and orange of the Rutaceae plant. It has good anti-cancer, antibacterial, anti-oxidation, lowering cholesterol, reducing capillary fragility, improving microcirculation and other biological activities, and is often used in medicine, cosmetics, food and other fields. [0003] According to research, various biological activities of flavonoids are based on antioxidant activity, which is related to anti-free radical or anti-lipid peroxidation. The special structure endows it with a series of unique chemical properties, such as complexation or electrostatic interaction with various metal ions, the characteristics of reducing...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Application Information

Patent Timeline
no application Login to view more
IPC IPC(8): C12P19/60
Inventor 杜理华罗锡平何锋凌慧敏杨文俊
Owner ZHEJIANG UNIV OF TECH
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap