CN1611508A - Process for preparing salicin - Google Patents
Process for preparing salicin Download PDFInfo
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- CN1611508A CN1611508A CN 200310105868 CN200310105868A CN1611508A CN 1611508 A CN1611508 A CN 1611508A CN 200310105868 CN200310105868 CN 200310105868 CN 200310105868 A CN200310105868 A CN 200310105868A CN 1611508 A CN1611508 A CN 1611508A
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- extraction
- preparation technology
- salicyl alcohol
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- alcohol glucoside
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Abstract
The invention relates to a kind of salicin and its manufacturing technology, which belongs to biology extraction field. The technology solution of the invention includes the steps in turn as follows: 1) Stock preparation: shatter with leaf into carven stock; 2) Hydrolysis and extraction: add basic matter into raw material for hydrolysis, and then extract with extraction agent in order to remove residue; 3) Concentration: get the semi-manufactured product containing salicin extractive material. The advantages of this industrial art can be described as follows: 1. acquirable raw material; 2. forthright industrial art; 3. high yield: the yield of the product is high, and according to production verification, the purity of salicin with refining step can achieve up to more than or equal to 99%; 4. low cost: the production of 1 kilogram with 95%n purity only sales a little more than upsi 3000.
Description
Affiliated technical field:
The present invention relates to the biological extraction field, be specifically related to a kind of salicyl alcohol glucoside preparation technology.
Background technology:
Salicaceae (Salicaceae) Salix (Salix) plant that distributes in the whole world has 500 kinds approximately, their mainly distribute areas, temperate zone in the Northern Hemisphere.China has 200 kinds approximately, white willow wherein (Salix alba L), weeping willow (Salix babylonica Linn.), Wu Liu (Salix cheilophila Schneid), Root of Littleleaf Willow (Salix hypoleuea Seem) etc. are used to be used as medicine, have clearing heat and detoxicating, dispel rheumatism, effect such as promoting blood circulation and removing blood stasis.Main component with the effect of being used as medicine is the salicyl alcohol glucoside that white willow, Root of Littleleaf Willow, weeping willow include, salicyl alcohol glucoside the research of chemistry and pharmacology report was arranged, but do not see the report of extraction process aspect up to now.
Summary of the invention:
The objective of the invention is to provide a kind of salicyl alcohol glucoside preparation technology.
Technical solution of the present invention, a kind of salicyl alcohol glucoside preparation technology: comprise the steps successively
(1) gets the raw materials ready: the withy leaf is ground into the segment raw material;
(2) hydrolysis is extracted: add alkaline matter and be hydrolyzed in raw material, extract with extraction agent then, remove residue;
(3) concentrate: obtain to contain salicyl alcohol glucoside medicinal extract work in-process.
The add-on of water is to get final product raw material is wetting in the above-mentioned steps (2).
Alkaline matter in the above-mentioned steps (2) is a calcium oxide, and the add-on of calcium oxide is 3～12% of a raw material weight.When calcium oxide is hydrolyzed as alkaline matter, in solution, can residue will be directly entered, the purity of product can be effectively improved with the impurity that calcium forms the insoluble calcium salt.
Alkaline matter in the above-mentioned steps (2) is the alkaline matter of sodium hydroxide or ammonium class.
In the above-mentioned steps (3), when extracting solution was concentrated, temperature was controlled at below 80 ℃, and being concentrated into medicinal extract proportion is 1.1～1.2.Temperature is controlled at below 80 ℃ can effectively guarantee product quality.
Above-mentioned preparation technology also comprises (4) purification step, and described purification step comprises extraction, crystallization and re-crystallization step.
In the above-mentioned purification step (4), extraction is with the medicinal extract water dissolution, and with not hydrophilic extraction agent extraction, extraction times is 3～4 times, and the consumption of each extraction agent is 1～1.5 times of the dissolving water consumption; Crystallization is with 15～30% of the extraction liquid simmer down to stoste volume after merging, places then and obtains coarse crystal; Recrystallization is to dissolve coarse crystallization with extraction agent, after the filtration filtrate is placed 12～24 hours, and crystallization obtains product.
5～10% the water that can add its volume during above-mentioned recrystallization in extraction agent participates in dissolving.Experiment shows that the product yield is higher when having water to participate in.
This technology has following advantage:
1. raw material is easy to get: with the branches and leaves that contain the very abundant sallow of salicyl alcohol glucoside is raw material, and said raw material can be the waste of beta pruning, does not destroy resource;
2. technology is simple and direct: the present invention is mainly by hydrolysis process, and is therefore simple, convenient, favorable reproducibility when being applied to produce;
3. productive rate height: the product yield height, through produce salicyl alcohol glucoside that checking obtains through purification step purity 〉=95%.
4. cost is low: 1 kilogram of purity is that the price of 95% product only is more than 3000 a yuan of Renminbi.
Description of drawings:
Accompanying drawing is a process flow sheet of the present invention.
Embodiment:
Below in conjunction with accompanying drawing the present invention is described in further detail.
Embodiment 1, and the present invention comprises the steps: successively
1. pulverize: 50 kilograms of white willow branches and leaves are ground into the segment raw material of 1～2cm, and the too big extraction of raw material is not thorough, and the too little then residue of raw material is difficult to remove;
2. hydrolysis, extraction: with 2.5 kilograms of calcium oxide, 15 kilograms in water adds in the raw material to be mixed thoroughly, and in the extractor of packing into, hydrolysis 3.5 hours makes in the raw material hydrolysis of salicyl alcohol glucoside derivative come out; The ethanol of adding 80% in extractor is 200 kilograms then, and refluxing extraction was filtered in 80 minutes, and residue extracts 2 times equally again, merging filtrate; Extracting solution carries out vacuum concentration, and temperature is controlled at below 80 ℃, and concentrated filtrate gets 30 kilograms of medicinal extract (being work in-process), and proportion is 1.1;
4. purification step: (1) extraction, medicinal extract is dissolved with 15 kg of water, add 15 kilograms of n-butanol extractions, tell extraction liquid propyl carbinol phase and water, add 15 kilograms of propyl carbinols again and extract in aqueous phase, repeat this extraction process 2 times, the combining extraction liquid propyl carbinol gets 65 kilograms mutually; (2) crystallization, extraction liquid are concentrated into 17% o'clock of stoste and stop to concentrate, and obtain coarse crystallization after the placement; (3) recrystallization, 0.2 kilogram of water and 3 kilograms of above-mentioned coarse crystallization of heat of solution of ethanol are filtered, and filtrate is placed 24 hours recrystallizations and is got 350 gram crystallizations, is 96.15% through the HPLC detection level.
Embodiment 2, and the present invention comprises the steps: successively
1. pulverize: the segment raw material that 50 kilograms of white willow branches and leaves is ground into 1～2cm;
2. hydrolysis, extraction: with 1.5 kilograms of sodium hydroxide, water adds in the raw material for 10 kilograms to be mixed thoroughly, in the extractor of packing into, and hydrolysis 1.5 hours; 200 kilograms of the ethanol of adding 80% in extractor, refluxing extraction was filtered in 40 minutes, and residue extracts 3 times equally again, merging filtrate; Extracting solution vacuum concentration, temperature are controlled at below 80 ℃, and concentrated filtrate gets 32 kilograms of medicinal extract, and proportion is 1.2;
4. purification step: (1) extraction, with the water dissolution of medicinal extract, add 20 kilograms of ethyl acetate extractions with 15 kilograms, tell extraction liquid and water, repeat to add 20 kilograms of ethyl acetate again and extract in aqueous phase, repeat this extraction 2 times, combining extraction liquid gets 150 kilograms; (2) crystallization, extraction liquid are concentrated into 25% o'clock of stoste and stop to concentrate, and obtain coarse crystallization after the placement; (3) recrystallization with 3.5 kilograms of above-mentioned coarse crystallization of heat of solution of ethanol, filters, and filtrate is placed 24 hours recrystallizations and got 360 gram crystallizations, is 95.10% through the HPLC detection level.
Claims (8)
1, a kind of salicyl alcohol glucoside preparation technology, it is characterized in that: comprise the steps successively
(1) gets the raw materials ready: the withy leaf is ground into the segment raw material;
(2) hydrolysis is extracted: add alkaline matter and be hydrolyzed in raw material, extract with extraction agent then, remove residue;
(3) concentrate: obtain to contain salicyl alcohol glucoside medicinal extract work in-process.
2, a kind of salicyl alcohol glucoside as claimed in claim 1 preparation technology, it is characterized in that: the add-on of water is to get final product raw material is wetting in the described step (2).
3, a kind of salicyl alcohol glucoside as claimed in claim 2 preparation technology, it is characterized in that: the alkaline matter in the described step (2) is a calcium oxide, the add-on of calcium oxide is 3～12% of a raw material weight.
4, a kind of salicyl alcohol glucoside as claimed in claim 2 preparation technology, it is characterized in that: the alkaline matter in the described step (2) is the alkaline matter of sodium hydroxide or ammonium class.
5, a kind of salicyl alcohol glucoside as claimed in claim 3 preparation technology, it is characterized in that: in the described step (3), when extracting solution was concentrated, temperature was controlled at below 80 ℃, being concentrated into medicinal extract proportion is 1.1～1.2.
6, as claim 3 or 5 described a kind of salicyl alcohol glucosides preparation technology, it is characterized in that: described preparation technology also comprises (4) purification step, and described purification step comprises extraction, crystallization and re-crystallization step.
7, a kind of salicyl alcohol glucoside as claimed in claim 6 preparation technology, tool is characterised in that: in the described purification step (4), extraction is with the medicinal extract water dissolution, with not hydrophilic extraction agent extraction, extraction times is 3～4 times, and the consumption of each extraction agent is 1～1.5 times of the dissolving water consumption; Crystallization is with 15～30% of the extraction liquid simmer down to stoste volume after merging, places then and obtains coarse crystal; Recrystallization is to dissolve coarse crystallization with extraction agent, after the filtration filtrate is placed 12～24 hours, and crystallization obtains product.
8, a kind of salicyl alcohol glucoside as claimed in claim 7 preparation technology, it is characterized in that: 5～10% the water that adds its volume during described recrystallization in extraction agent participates in dissolving.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 200310105868 CN1261443C (en) | 2003-10-30 | 2003-10-30 | Process for preparing salicin |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 200310105868 CN1261443C (en) | 2003-10-30 | 2003-10-30 | Process for preparing salicin |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1611508A true CN1611508A (en) | 2005-05-04 |
| CN1261443C CN1261443C (en) | 2006-06-28 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN 200310105868 Expired - Fee Related CN1261443C (en) | 2003-10-30 | 2003-10-30 | Process for preparing salicin |
Country Status (1)
| Country | Link |
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| CN (1) | CN1261443C (en) |
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102079764A (en) * | 2009-12-01 | 2011-06-01 | 汉中秦赢生物科技有限责任公司 | Method for preparing medicinal raw material salicin from white willow branch bark |
| CN102453061A (en) * | 2010-11-03 | 2012-05-16 | 张守力 | Method for extracting salicin |
| CN102558254A (en) * | 2010-12-30 | 2012-07-11 | 成都华高药业有限公司 | Extract of willow barks or willow branches and method for preparing salicin |
| CN102731587A (en) * | 2011-12-25 | 2012-10-17 | 大兴安岭林格贝有机食品有限责任公司 | Method for extracting salicin from white willow bark |
| CN102863483A (en) * | 2012-10-12 | 2013-01-09 | 成都乾坤动物药业有限公司 | Preparation process of salicin comparison product |
| CN104262421A (en) * | 2014-08-08 | 2015-01-07 | 图木舒克市昆神植物提取有限责任公司 | Process for extracting salicin from populus euphratica fallen leaves |
| CN106279302A (en) * | 2016-08-18 | 2017-01-04 | 三原金瑞生物工程有限公司 | The method extracting salicoside from Willow bark and the extract obtained |
| CN106957346A (en) * | 2017-01-12 | 2017-07-18 | 南阳理工学院 | The method that salicin is produced using diversiform-leaved poplar leaf |
| CN111647025A (en) * | 2020-06-18 | 2020-09-11 | 甘肃天顺植物科技有限公司 | Method for extracting, separating and refining salicin from willow |
-
2003
- 2003-10-30 CN CN 200310105868 patent/CN1261443C/en not_active Expired - Fee Related
Cited By (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102079764B (en) * | 2009-12-01 | 2013-04-17 | 汉中秦赢生物科技有限责任公司 | Method for preparing medicinal raw material salicin from white willow branch bark |
| CN102079764A (en) * | 2009-12-01 | 2011-06-01 | 汉中秦赢生物科技有限责任公司 | Method for preparing medicinal raw material salicin from white willow branch bark |
| CN102453061A (en) * | 2010-11-03 | 2012-05-16 | 张守力 | Method for extracting salicin |
| CN102453061B (en) * | 2010-11-03 | 2014-09-10 | 张守力 | Method for extracting salicin |
| CN102558254B (en) * | 2010-12-30 | 2015-05-20 | 成都华高药业有限公司 | Extract of willow barks or willow branches and method for preparing salicin |
| CN102558254A (en) * | 2010-12-30 | 2012-07-11 | 成都华高药业有限公司 | Extract of willow barks or willow branches and method for preparing salicin |
| CN102731587A (en) * | 2011-12-25 | 2012-10-17 | 大兴安岭林格贝有机食品有限责任公司 | Method for extracting salicin from white willow bark |
| CN102731587B (en) * | 2011-12-25 | 2015-04-22 | 大兴安岭林格贝有机食品有限责任公司 | Method for extracting salicin from white willow bark |
| CN102863483A (en) * | 2012-10-12 | 2013-01-09 | 成都乾坤动物药业有限公司 | Preparation process of salicin comparison product |
| CN104262421A (en) * | 2014-08-08 | 2015-01-07 | 图木舒克市昆神植物提取有限责任公司 | Process for extracting salicin from populus euphratica fallen leaves |
| CN104262421B (en) * | 2014-08-08 | 2017-03-08 | 图木舒克市昆神植物提取有限责任公司 | The technique extracting salicoside from Populus euphratica fallen leaves |
| CN106279302A (en) * | 2016-08-18 | 2017-01-04 | 三原金瑞生物工程有限公司 | The method extracting salicoside from Willow bark and the extract obtained |
| CN106957346A (en) * | 2017-01-12 | 2017-07-18 | 南阳理工学院 | The method that salicin is produced using diversiform-leaved poplar leaf |
| CN111647025A (en) * | 2020-06-18 | 2020-09-11 | 甘肃天顺植物科技有限公司 | Method for extracting, separating and refining salicin from willow |
| CN111647025B (en) * | 2020-06-18 | 2023-05-02 | 甘肃天顺植物科技有限公司 | Method for extracting, separating and refining salicin from willow |
Also Published As
| Publication number | Publication date |
|---|---|
| CN1261443C (en) | 2006-06-28 |
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Granted publication date: 20060628 Termination date: 20131030 |