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

Method for preparing ethyl nervonate by using acer-trunctum-bung oil as raw material

A technology of ethyl nervate and Yuanbaofeng, which is applied in fatty acid esterification, carboxylate preparation, chemical instruments and methods, etc., can solve the problem of many six-stage molecular distillation stages, unsuitable for technological production and low separation efficiency. and other problems, to achieve the effect of good separation effect, favorable for industrial production and small product denaturation

Inactive Publication Date: 2017-03-15
武汉藤欣生物工程有限公司
View PDF6 Cites 3 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The patent steps are cumbersome, the yield is low, the pollution is large, and a large amount of organic solvent is used, the separation efficiency is low, the production cost is high, and it is not suitable for technological production
[0006] Chinese patent (disclosure date: January 19, 2011, announcement number: CN101092344B) discloses a method for extracting nervous acid from maple ingot oil by molecular distillation technology. This patent first converts maple ingot oil into fatty acid ethyl ester, Then through the six-stage molecular distillation, ethyl nervate is proposed, but the six-stage molecular distillation has many stages, low efficiency, high energy consumption, and finally only 50% content of ethyl nervate can be obtained.
[0007] Chinese patent (publication date: August 31, 2011, announcement number: CN101429112B) discloses a method for separating the mixture of nervous acid and erucic acid from the molecular distillation of Yuanbao maple oil. It also uses six-stage molecular distillation technology with many stages. , low efficiency, high energy consumption, and finally only 50% ethyl nervate can be obtained. The product is a mixture of ethyl nereunate and ethyl erucate, and subsequent purification steps are required to obtain high-content ethyl nereunate

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 ethyl nervonate by using acer-trunctum-bung oil as raw material
  • Method for preparing ethyl nervonate by using acer-trunctum-bung oil as raw material
  • Method for preparing ethyl nervonate by using acer-trunctum-bung oil as raw material

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0033] 1) 1000g Ingot Maple Oil and 400ml of absolute ethanol and 40ml of sodium ethylate (20% sodium ethylate in ethanol) were subjected to a transesterification reaction at 75°C for 2 hours. After the reaction, unreacted ethanol was reclaimed. Stand still to remove glycerin, alkali and a small amount of ethanol, then wash with water until neutral, dry and dehydrate in vacuum to obtain Ingot Maple Oil Ethyl Ester;

[0034] 2) the ingot maple oil ethyl ester in the step 1) is removed through the first-stage rectification to remove the first-stage light component, and obtain the first-stage heavy component;

[0035] 3) removing the second-stage light components from the first-stage heavy components in step 2) through second-stage rectification to obtain the second-stage heavy components;

[0036] 4) removing the third-level light component through the third-level rectification of the second-level heavy component in step 3), to obtain the third-level heavy component;

[0037] 5) ...

Embodiment 2

[0043] 1) Put 1000g of maple ingot oil, 600ml of absolute ethanol and 10g of sodium hydroxide at 80°C for 1 hour for transesterification. After the reaction, recover the unreacted ethanol and let it stand to remove glycerin, alkali and A small amount of ethanol, then washed with water until neutral, vacuum dried and dehydrated to obtain Ingot Maple Oil Ethyl Ester;

[0044] 2) the ingot maple oil ethyl ester in the step 1) is removed through the first-stage rectification to remove the first-stage light component, and obtain the first-stage heavy component;

[0045] 3) removing the second-stage light components from the first-stage heavy components in step 2) through second-stage rectification to obtain the second-stage heavy components;

[0046] 4) removing the third-level light component through the third-level rectification of the second-level heavy component in step 3), to obtain the third-level heavy component;

[0047] 5) The third stage heavy component in step 4) is sep...

Embodiment 3

[0053] 1) Put 1000g of maple ingot oil, 500ml of absolute ethanol and 8g of potassium hydroxide at 70°C for 1.5 hours for transesterification. After the reaction, recover the unreacted ethanol and let it stand to remove glycerin, alkali and A small amount of ethanol, then washed with water until neutral, vacuum dried and dehydrated to obtain Ingot Maple Oil Ethyl Ester;

[0054] 2) the ingot maple oil ethyl ester in the step 1) is removed through the first-stage rectification to remove the first-stage light component, and obtain the first-stage heavy component;

[0055] 3) removing the second-stage light components from the first-stage heavy components in step 2) through second-stage rectification to obtain the second-stage heavy components;

[0056] 4) removing the third-level light component through the third-level rectification of the second-level heavy component in step 3), to obtain the third-level heavy component;

[0057] 5) The third stage heavy component in step 4) i...

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 preparing ethyl nervonate by using using acer-trunctum-bunge oil as a raw material. The method comprises the following steps: carrying out an interesterification reaction on the acer-trunctum-bunge oil and ethanol, and obtaining acer-trunctum-bunge oil ethyl ester; removing a first-stage light component from the acer-trunctum-bunge oil ethyl ester by first-stage rectification, and obtaining a first-stage heavy component; removing a second-stage light component from the first-stage heavy component by second-stage rectification, and obtaining a second-stage heavy component; removing a third-stage light component from the second-glass heavy component by third-stage rectification, and obtaining a third-stage heavy component; purifying the third-stage heavy component, and then obtaining the ethyl nervonate. Compared with the molecular distillation in the prior art, the three-stage rectification adopted by the method for preparing the ethyl nervonate, which is provided by the invention, has higher efficiency and lower energy consumption; moreover, the content of a product is up to 90%; the quality of the product is good; the method is beneficial to industrialized production, and has quite high practicability.

Description

technical field [0001] The invention relates to the field of separation and preparation of chemical raw materials, in particular to a method for preparing ethyl nervate from ingot maple oil. Background technique [0002] Nervous acid was first discovered in the nervous tissue of mammals, so it is named as nervonic acid, and its chemical name is cis-15-tetradecenoic acid. It is an omega-9 long-chain monounsaturated fatty acid with a molecular weight of 366.62 , with a melting point of 42-43°C and a density of 0.887g / cm 3 , The flash point is 375.8°C, and the nervonic acid is white flaky crystal at room temperature. Nervous acids are mainly present in human brain proteins, retina, sperm and nerve tissues in the form of glycosphingolipids and sphingomyelin. Foreign studies have shown that nervonic acid is the core natural component of brain nerve cells and nerve tissues. It is the special substance found in the world that can promote the repair and regeneration of damaged ner...

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): C07C67/03C07C67/54C07C69/533C11C3/10
CPCC07C67/03C07C67/54C11C3/10C07C69/533
Inventor 周小波
Owner 武汉藤欣生物工程有限公司
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