Unlock instant, AI-driven research and patent intelligence for your innovation.

Method for preparing inulin short-chain fatty acid ester

A technology of fatty acid ester and fatty acid anhydride, which is applied in the field of preparation of inulin short-chain fatty acid ester, can solve problems such as low esterification rate, uncontrollable reaction, and environmental pollution, and achieves improved yield, simple preparation method, and high yield high rate effect

Inactive Publication Date: 2018-02-09
YANTAI INST OF COASTAL ZONE RES CHINESE ACAD OF SCI +1
View PDF5 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] In order to solve the problems of uncontrollable reaction, low esterification rate and environmental pollution in the aqueous phase preparation method of inulin short-chain fatty acid ester in the prior art, the present invention provides a preparation method of inulin short-chain fatty acid ester

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 preparing inulin short-chain fatty acid ester
  • Method for preparing inulin short-chain fatty acid ester
  • Method for preparing inulin short-chain fatty acid ester

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0028] The preparation of embodiment 1 inulin propionate

[0029] Add inulin to pyridine at 40°C to dissolve, stir during the dissolution process, and stir for 20 minutes to make the concentration of inulin in pyridine reach 30%, then add propionic anhydride dropwise to the pyridine solution, when propionic anhydride and When the molar ratio of inulin is 3:1, the dropwise addition is completed, the reaction time of the esterification reaction is 24h, and the reaction temperature is 40°C. After the reaction is completed, add deionized water for treatment, extract twice with dichloromethane, and organic The phases were sequentially extracted with saturated sodium chloride solution, saturated sodium bicarbonate solution and saturated sodium chloride solution, concentrated by rotary evaporation, and dried by a vacuum pump to obtain the product inulin propionate. The yield of the product was 87%, and the degree of esterification was is 2.86.

Embodiment 2

[0030] The preparation of embodiment 2 inulin propionate

[0031] Add inulin to pyridine at 60°C to dissolve, stir during the dissolution process, and stir for 10 minutes to make the concentration of inulin in pyridine reach 15%, then add propionic anhydride dropwise to the pyridine solution, when propionic anhydride and When the molar ratio of inulin is 1:1, the dropwise addition is completed, the reaction time of the esterification reaction is 30h, and the reaction temperature is 20°C. After the reaction is completed, add deionized water for treatment, extract twice with dichloromethane, and The phases were sequentially extracted with saturated sodium chloride solution, saturated sodium bicarbonate solution and saturated sodium chloride solution, concentrated by rotary evaporation, and dried by a vacuum pump to obtain the product inulin propionate, and the yield of the product was 82%, and the degree of esterification was is 2.26.

Embodiment 3

[0032] The preparation of embodiment 3 inulin propionate

[0033]Add inulin to pyridine at 20°C to dissolve, stir during the dissolution process, and stir for 20 minutes to make the concentration of inulin in pyridine reach 40%, then add propionic anhydride dropwise to the pyridine solution, when propionic anhydride and When the molar ratio of inulin is 5:1, the dropwise addition is completed, the reaction time of the esterification reaction is 12h, and the reaction temperature is 60°C. After the reaction is completed, add deionized water for treatment, extract twice with dichloromethane, and organic The phases were sequentially extracted with saturated sodium chloride solution, saturated sodium bicarbonate solution and saturated sodium chloride solution, concentrated by rotary evaporation, and dried by a vacuum pump to obtain the product inulin propionate. The yield of the product was 83%, and the degree of esterification was is 2.50.

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 relates to the field of chemical synthesis and discloses a method for preparing an inulin short-chain fatty acid ester. According to the preparation method, pyridine serves as an organicphase to dissolve inulin, the dissolved inulin and an esterifying agent short-chain fatty acid anhydride or acyl chloride compounds react to undergo esterification reaction, and the inulin short-chain fatty acid ester is generated. The preparation method can effectively reduce generation of by-products, the obtained inulin short-chain fatty acid ester is high in yield, and the preparation methodis simple and favorable for industrial production.

Description

technical field [0001] The invention relates to the field of chemical synthesis, in particular to a preparation method of inulin short-chain fatty acid ester. Background technique [0002] Inulin is a natural fructan. Some scholars at home and abroad have carried out various chemical modifications such as sulfation, carboxymethylation, and alkylation on inulin, which broadened its application fields. Through structural modification, inulin can be changed. The spatial structure, molecular weight and substituent type, number and position of the powder affect its activity. Among them, the inulin short-chain fatty acid ester (as shown in formula I) is formed by the inulin hydroxyl group and the short-chain fatty acid anhydride or acid chloride. Produced by esterification reaction. Inulin short-chain fatty acid esters can be fermented by some bacteria in the colon to produce short-chain fatty acid (SCFA). The mechanism of SCFA’s impact on the human body mainly has the following ...

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): C07H15/06C07H1/00C08B37/18
CPCC07H1/00C07H15/06C08B37/0051
Inventor 衣悦涛朱晓振任世斌
Owner YANTAI INST OF COASTAL ZONE RES CHINESE ACAD OF SCI