Novel method used for synthesizing cholesterol

A technology of cholesterol and new method, applied in the field of synthesizing cholesterol, can solve the problems of large consumption of raw and auxiliary materials, uneconomical, long steps, etc., and achieve the effects of reducing unit consumption, low cost and improving yield

Inactive Publication Date: 2017-05-10
HUNAN KEREY BIOTECH
View PDF4 Cites 17 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0006] The existing method uses turmeric extract saponin as raw material to obtain cholesterol (01) through 6-step reaction. The step

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
  • Novel method used for synthesizing cholesterol
  • Novel method used for synthesizing cholesterol

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0030] A new method for synthesizing cholesterol, comprising the following steps:

[0031] (1) At room temperature, add 1000ml of dichloromethane to a 2000L reaction glass reaction bottle, stir, add 37g of imidazole, add 200g of stigmasterol 02, cool down in an ice-water bath to below 10°C, slowly add 59g of trimethylchlorosilane dropwise, After the addition was completed, the internal temperature was controlled at 20°C and the reaction was incubated for 1.5 hours. After the reaction, wash with water until neutral, add 400ml of tap water, concentrate at normal pressure until there is no solvent smell, cool down to below 40°C, filter, wash with water, drain, and dry to obtain 229.21g of compound 03 with a molar yield of 97.36%.

[0032] (2) Dissolve 20 g of compound 03 in 1000 mL of dichloromethane, cool down to -70 °C, slowly bubble in ozone, react for 2 hours, the reaction is complete, the reaction is moved to room temperature, add 18.4 g of zinc powder and 20 mL of Glacial ...

Embodiment 2

[0036] The synthesis method is the same as in Example 1, the only difference is that in this example, the amount of imidazole and trimethylchlorosilane in step (1) of Example 1 were adjusted to 40g and 64g respectively to obtain 229.05g of compound 03, with a molar yield 97.29%; the amount of zinc powder in step (2) was adjusted to 21.5g, and 11.56g of compound 04 was obtained, with a molar yield of 84.95%; triphenylphosphine, 1-chloro-3-methylbutyl The consumption of alkane, potassium tert-butoxide, and 30% industrial concentrated hydrochloric acid are adjusted to 94g, 39g, 48g, and 58g respectively to obtain 55.05g compound 05, with a molar yield of 90.98%; 1% palladium carbon catalyst in step (4) and ammonium acetate were adjusted to 4g and 8g, respectively, to obtain 184.21g of cholesterol 01, and the molar yield was 91.63%.

Embodiment 3

[0038]The synthesis method is the same as in Example 1, the only difference is that in this example, the amount of imidazole and trimethylchlorosilane in step (1) of Example 1 were adjusted to 43g and 69g respectively, and 228.34g of compound 03 was obtained, with a molar yield 96.99%; the amount of zinc powder in step (2) was adjusted to 24.5g, and 11.50g of compound 04 was obtained, with a molar yield of 84.51%; triphenylphosphine, 1-chloro-3-methylbutane in step (3) , Potassium tert-butoxide consumption is adjusted to be 125g, 58g and 42.5g respectively, and 30% industrial concentrated hydrochloric acid is changed into the industrial concentrated sulfuric acid of 32g, obtains 54.39g compound 05, molar yield 90.78%; 1 in step (4) % palladium carbon catalyst and ammonium acetate were adjusted to 6g and 12g respectively, to obtain 184.05g cholesterol 01, and the molar yield was 91.55%.

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 novel method used for synthesizing cholesterol. The novel method comprises following steps: 1, stigmasterol 02 is dissolved in an organic solvent I, and is subjected to silicon etherification reaction with trimethylchlorosilane under the effect of a catalyst, and a compound 03 is obtained via water washing and condensation; 2, the compound 03 is dissolved in an organic solvent II for ozone oxidation, zinc powder and acetate acid gracial are added for reduction, after reduction, filtering, washing, and condensation are carried out so as to obtain a compound 04; 3, triphenylphosphine is reacted with 1-halogenated-3-methyl butane so as to obtain 3-methyl butyl triphenyl halogenated phosphorus, the 3-methyl butyl triphenyl halogenated phosphorus is added into an aprotic solvent, a strong base is added, wittig reaction with a compound 4 is carried out, and neutralizing, condensation, and filtering are carried out so as to obtain a compound 05; 4, the compound 05 is subjected to selective hydrogenation in a solvent III under the action of a catalyst and a passivator, and filtering, condensation, and crystallization are carried out so as to obtain cholesterol 01. The novel method is simple; raw materials are cheap; the novel method is economic and is friendly to the environment, and is convenient for industrialized production.

Description

technical field [0001] The invention belongs to the field of organic chemistry, and in particular relates to a new method for synthesizing cholesterol. Background technique [0002] Cholesterol, also known as cholesterol, is a derivative of cyclopentane polyhydrophenanthrene. As early as the 18th century, people had discovered cholesterol from gallstones. In 1816, the chemist Bencher named this lipid-like substance cholesterol. Cholesterol is widely present in animals, especially in brain and nerve tissue, and is also high in kidney, spleen, skin, liver and bile. Its solubility is similar to that of fat, insoluble in water, and easily soluble in solvents such as ether and chloroform. Cholesterol is an indispensable and important substance in animal tissue cells. It not only participates in the formation of cell membranes, but also is a raw material for the synthesis of bile acids, vitamin D and steroid hormones. [0003] At present, cholesterol is mainly extracted from th...

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): C07J9/00
CPCC07J9/00
Inventor 左前进
Owner HUNAN KEREY BIOTECH
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