Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Synthetic method for rebaudioside R

A technology of stevioside and compound, which is applied in the field of synthesis of stevioside R, can solve problems such as methods to be optimized, and achieve the effects of ensuring synthesis efficiency, increasing synthesis efficiency, and reducing synthesis steps

Active Publication Date: 2020-02-21
JIANGXI NORMAL UNIV
View PDF4 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Therefore, the method of introducing the C13 sugar chain of stevioside R needs to be optimized

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
  • Synthetic method for rebaudioside R
  • Synthetic method for rebaudioside R
  • Synthetic method for rebaudioside R

Examples

Experimental program
Comparison scheme
Effect test

preparation example Construction

[0056] The preparation method of some compounds in the present invention is as follows:

[0057] (1) Preparation method of compound 1

[0058]

[0059] Starting from glucose, compound 1 was obtained with a yield of 70% after three steps of reaction. .

[0060] (2) Preparation method of compound 2

[0061]

[0062] Compound 11 was prepared by referring to the method in J.Carbohydr.Chem.2007, 26, 61-82, and the 4-position hydroxyl group was dissolved in compound 11 (5.9g, 19.9mmol) in anhydrous DMF (25mL), and added in batches at 0°C NaH (0.96 g, 40.0 mmol). N 2 After stirring for 20 minutes under the atmosphere, NapBr (5.27 g, 23.8 mmol) was added to the reaction mixture, and stirred at this temperature for 3 hours. The reaction was quenched with water, diluted with ethyl acetate, washed with water and brine, then washed with anhydrous Na 2 SO 4 Drying, filtration, and concentration under reduced pressure gave a crude product, which was further purified by silica g...

Embodiment 1

[0070] Step 1: 4-Methoxyphenyl-2,3-di-O-(2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyl)-4-O -(2-Naphthylmethyl)-β-D-xylopyranoside (3)

[0071] To the anhydrous CH of 1 (280mg, 0.38mmol) and 2 (50mg, 0.126mmol) 2 Cl 2 (1 mL) activated powdered 4A molecular sieves (80 mg) were added to the solution. The resulting suspension was stirred at the same temperature for 30 minutes, then cooled to -40°C, and TMSOTf (14.4 μL, 0.08 mmol) was added thereto. After the reaction solution was stirred at -40°C for another 1 hour, Et 3 N to quench the reaction. After filtration, it was concentrated under reduced pressure, and the resulting residue was purified by silica gel column chromatography to obtain Compound 3 (150 mg, 77%) as a colorless foam. [α] D 25 =+70.8(c 0.5, CHCl 3 ); 1 H NMR (400MHz, CDCl 3 )δ8.33(d, J=7.2Hz, 2H), 8.26(d, J=7.2Hz, 2H), 7.98-7.28(m, 47H), 6.85(d, J=9.2 Hz, 2H), 6.58( d, J=8.8Hz, 2H), 5.87(q, J=9.6Hz, 2H), 5.66-5.53(m, 4H), 5.01(d, J=12.4Hz, 1H), 4.92(d, J=8...

Embodiment 2

[0083] The method preparation of reference example. The difference is:

[0084] In step (1), the mol ratio of Compound 1 and Compound 2 is 1:1, and the mol ratio of TMSOTf and Compound 2 is 0.7:1;

[0085] In step (2a), the volume ratio of acetonitrile and the buffer solution is 1:1, the molar ratio of CAN and compound 3 is 5:1, and the concentration of compound 3 in the mixed solution is 0.1mol / L;

[0086] In step (2b), the hemiacetal intermediate, ABzOH, iPr 2 The molar ratio of NEt, DMAP and EDCI is 1:1.5:4:2:4;

[0087] In step (3), Ph 3 wxya 2 The molar ratio of compound 4 and compound 4 is 0.1:1, and the molar ratio of compound 4 and compound 5 is 1:1; the concentration of compound 5 in acetonitrile is 0.01mol / L.

[0088] In step (4), the molar ratio of compound 6, HOAc and TBAF is 1:4:2; the concentration of compound 6 in the solvent is 0.02mol / L;

[0089] In step (5), the volume ratio of chloroform and water is 1:1.5, compound 8, K 2 CO 3 , TBAB and the molar r...

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 preparation method for rebaudioside R for the first time. The method adopts a convergent synthetic route, and starts from raw materials 1 and 2 to obtain the rebaudioside R with a total yield of 19.4% through six-step reactions. The method provides a concise and implementable strategy for the efficient and diverse synthesis of the compounds.

Description

[0001] field of invention [0002] The invention belongs to the field of organic synthesis and relates to a synthesis method of stevioside R. Background technique [0003] Stevioside is a kaurane-type diterpene disaccharide chain glycoside mixture extracted from the leaves of Stevia rebaudiana Bertoni. Its sweetness is 150-300 times that of sucrose, and it is a strong sweetener. Compared with other sweeteners, it has low cost of use (compared with sucrose, which can reduce the cost by more than 60%), stable properties (high temperature and acid-base resistance), and high safety in use (long-term toxicology and pharmacological studies have shown that the main component of stevioside It does not participate in metabolism in the body, does not accumulate, has no toxicity and genetic hazards, and does not cause changes in blood sugar and insulin levels after ingestion, so it is also suitable for diabetic patients. Its safety has passed the US Food and Drug Administration The GRAS...

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
Patent Type & Authority Applications(China)
IPC IPC(8): C07H1/00C07H15/256A23L27/30
CPCA23L27/36A23V2002/00C07H1/00C07H15/256A23V2200/132A23V2200/30Y02P20/55
Inventor 孙建松文国恩张庆举夏剑辉
Owner JIANGXI NORMAL UNIV
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products

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

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com