CN1727363A - N-substituted carboxymethyl chitosan and preparation method thereof - Google Patents
N-substituted carboxymethyl chitosan and preparation method thereof Download PDFInfo
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- CN1727363A CN1727363A CN 200510044307 CN200510044307A CN1727363A CN 1727363 A CN1727363 A CN 1727363A CN 200510044307 CN200510044307 CN 200510044307 CN 200510044307 A CN200510044307 A CN 200510044307A CN 1727363 A CN1727363 A CN 1727363A
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Abstract
A kind of N-substituted carboxymethyl chitosan is to be reacted in the aqueous solution by cm-chitosan and substituted salicylic aldehydes to obtain the schiff bases intermediate, again through NaBH
4Obtain the N-substituted carboxymethyl chitosan of different molecular weight after the reduction.Studies show that, successfully synthesized N-2-hydroxyl-5-chlorophenylmethyl cm-chitosan and N-2-hydroxyl-N-substituted carboxymethyl chitosan derivatives such as 5-oil of mirbane methyl cm-chitosan with preparation method of the present invention.Amino group substitution degree in this analog derivative chitosan is up to 34.3-56.5%, and is water-soluble better, and has bacteriostatic activity preferably, can be widely used in fields such as medicine or agricultural chemicals.
Description
Technical field
The invention belongs to the marine chemical industry field of engineering technology, relate to a kind of new N-substituted carboxymethyl chitosan compound and technology of preparing thereof.
Background technology
The agricultural chemicals initiative is a hi-tech, engineering with high investment, high risk, and a kind of new variety of present every exploitation approximately need the 5-8 year, hundred million dollars of expensive 1-2, screen the compound about 100,000, and along with the requirement of environmental problem, these numerals also will increase.The stand-alone development new variety of having the ability at present have only An Wante, Bayer, Meng Shan all to wait international big agricultural chemicals company.How researching and developing the novel pesticide of China, is the severe problem that faces under situation about being gradually improved along with accession to WTO and intellectual property protection.
At the practical situation in international sterilant market and the direction of research, the situation of the active and appearance of each series bactericidal agent.Simultaneously according to our technical strength and economic strength, cooperate with the offshore company or take " me-too chemistry " to be considered to effectively formulate approach.Promptly on present existing sterilant basis, row is theoretical that existing existing group with germicidal action is carried out the derivatize modification for thought that connects with substructure or biology etc., develops the secondary lead compound with better fungicidal activity and easier degraded.This initiative approach is with clearly defined objective, laborsaving saving money, and also opportunity of success is more.
Chitosan (Chitosan) be a kind of extensively be present in occurring in nature renewable, have no side effect, the natural glycosaminoglycan that biocompatibility and degradation property are good, himself and derivative thereof have physiology, the pharmacological function character of many uniquenesses, are widely used in the multiple industry fields such as medicine, food, agricultural, daily use chemicals, environmental protection.Structure that chitosan itself is special and character have sterilization, bacteriostatic activity, and nontoxic, free of contamination characteristic, and the object that can be used as modification is in the hope of developing the secondary lead compound.Reactive group on the chitosan molecule---hydroxyl and amino can be used as the effect group when modifying.Substituted benzene ring has a wide range of applications in existing agricultural bactericide, have the good sterilization effect, there is a free amino C-2 position of chitosan, can react with aldehyde radical, access has the group of different activities, is the novel direction that chitosan is used on agricultural.
Cm-chitosan has good water-soluble and bacteriostatic activity preferably, but the product that seldom has pair cm-chitosan further to modify, the substituting group of cm-chitosan inserts the hydroxyl and the amino of chitosan, but amino substitution value has only 0.1-0.2 (Chen Lingyun, Du Yumin, Liu Yi, the structure of cm-chitosan and anti-microbial property research, Wuhan University's journal (natural science edition), 2000,45,191-1 94), reach 97% chitosan for deacetylation, 80% the amino of also having an appointment can be participated in reaction, so, chitosan is further modified, have very big DEVELOPMENT PROSPECT.At the bactericidal activity of chitosan and cm-chitosan, do not participate in the hydroxyl and the amino of reaction in cm-chitosan yet and modify, insert group with fungicidal activity, be expected to obtain water miscible active chitosan derivative.
Summary of the invention
The object of the present invention is to provide the high chitosan derivatives of a kind of good water solubility and biological activity.
Another object of the present invention provides a kind of method of the chitosan derivatives from the high amino group substitution degree of Preparation of Chitosan.
The invention provides a kind of method for preparing general formula (I) compound.
Formula (1)
Y represents an active group in the formula
Preparation method of the present invention comprises following key step:
(1), the substituted salicylic aldehydes reaction with cm-chitosan and general formula (II) obtains the schiff bases intermediate;
Formula (II)
(2), use NaBH
4Reduction makes general formula (I) compound;
(3), obtain throw out, the 3-6 that used organic solvent volume is the liquor capacity total amount times in the reaction product impouring organic solvent;
(4), after filtration, separate, with alcoholic solvent purification by liquid extraction in cable type extractor according, obtain the N-substituted carboxymethyl chitosan of formula (I).
In preparation method of the present invention, as formula (II) compound of starting material, wherein the Y in the Y cotype (I) represents an active group, represents chlorine atom, nitro here; Cm-chitosan as starting material can be prepared from chitosan with known method, as obtaining cm-chitosan with chitosan and chloroacetate reaction.The molecular weight of used here chitosan is between the 1-70 ten thousand, and deacetylation is 80-100%.
In preparation method of the present invention, the reaction of cm-chitosan and substituted salicylic aldehydes and reduction reaction are all carried out homogeneous reaction in the aqueous solution.The mol ratio of cm-chitosan and substituted salicylic aldehydes is 1: 3-1: 5, and the reaction times is 1-3 hour; Substituted salicylic aldehydes and NaBH
4Mol ratio be 1: 1.5-1: 3, the reaction times is 2-4 hour.It is N-substituted carboxymethyl chitosan crude product that reaction product after the reduction then obtains throw out in a kind of organic solvent of impouring, and it is selected from acetone or 80% above ethanol said organic solvent, and the 3-6 that used organic solvent volume is the liquor capacity total amount doubly.In apparatus,Soxhlet's, promptly obtained the N-substituted carboxymethyl chitosan of formula (I) after the filtering separation in purification by liquid extraction 24-72 hour with dehydrated alcohol.
The formula of so making (I) compound, with the infrared spectra affirmation that performs an analysis, the carboxymethyl chitosan glycan molecule combines effectively with the group of access and forms N-substituted carboxymethyl chitosan.Wherein Fan Ying amino of chitosan group does not comprise by methylol replacing part, accounts for the 34.3-56.5% of amino total amount in the chitosan;
N-2-hydroxyl-5-chlorophenylmethyl the cm-chitosan that obtains by preparation method of the present invention is a pale yellow powder, Fan Ying amino of chitosan group wherein, do not comprise by methylol replacing part, account for the 34.3-56.5% of amino total amount in the chitosan, its characteristic infrared absorption spectrum (cm
-1): 3468.86,2924.61,1654.62,1614.44,1465.15,1004.90,866.00,722.64.
The N-2-hydroxyl of producing-5-oil of mirbane methyl cm-chitosan is pale yellow powder; Wherein Fan Ying amino of chitosan group does not comprise by methylol replacing part, accounts for the 34.3-56.5% of amino total amount in the chitosan; Its characteristic infrared absorption spectrum (cm
-1): 3516.48,1643.08,1512.25,1464.90,871.12,697.27.
Description of drawings
Fig. 1 is the infrared spectrum of chitosan; Its characteristic infrared (cm
-1): 3447.07,2920.17,2875.94,1600.03,1423.38,1382.43,1154.98,1081.84,897.85.
The infrared spectrum of Fig. 2 cm-chitosan; Its characteristic infrared (cm
-1): 3450.12,2945.40,1614.96,1412.88,1320.50,1066.24.
Fig. 3 is the infrared spectrum of the cm-chitosan of chlorine substituted-phenyl; Its characteristic infrared (cm
-1): 3468.86,2924.61,1654.62,1614.44,1465.15,1004.90,866.00,722.64.
Fig. 4 is the infrared spectrum of the cm-chitosan of nitro substituted-phenyl; Its characteristic infrared (cm
-1): 3516.48,1643.08,1512.25,1461.90,871.12,697.27.
Embodiment
The invention will be further described with by way of example more below, provides implementation detail of the present invention, but be not intended to limit protection scope of the present invention.
Stir down, soluble in water cm-chitosan, add mol ratio at normal temperatures and be 1: 4 substituted salicylic aldehydes, reaction is 2 hours under the magnetic agitation, adds the NaBH of 1.5 times of used aldehyde molar masss then
4Reduce, obtain precipitation in the product impouring acetone, filter the back and extracted in apparatus,Soxhlet's 24 hours with ethanol, lyophilize under the vacuum obtains N-substituted carboxymethyl chitosan.Amino group in the chitosan does not comprise by methylol replacing part that its substitution value is the 34.3-56.5% of amino total amount.
The present invention will be further described to use several embodiment below again
1g polymer cm-chitosan (Mw=7.0 * 10
5) be dissolved in the 50ml distilled water, add 2.4 gram 5-chloro-salicylic aldehydes, magnetic agitation, normal temperature reaction down adds 0.85 gram NaBH after 1 hour
4(10% solution) reaction 2 hours in the ethanol of 3 times of volumes 90% of impouring, extracted in soxhlet's extractor 24 hours with dehydrated alcohol behind the sedimentation and filtration then, and vacuum lyophilization promptly obtains the high molecular cm-chitosan that 2-hydroxyl-5-chlorophenylmethyl replaces.
This compound is identified with infrared spectra, at 1654.62cm
-1The place is the absorption peak of secondary amine formation vibration, 1465.15cm
-1Be the skeleton stretching vibration of phenyl ring, 722.64cm
-1Stretching vibration absorption peak for C-Cl proves the formation of target product.
1g hangs down molecule cm-chitosan (Mw=1.0 * 10
4) be dissolved in the 50ml distilled water, add 4.2 gram 5-nitrosalicylaldehydes, magnetic agitation, normal temperature reacted 3 hours down, added 2.84 gram NaBH then
4(10% solution) reaction 4 hours in the acetone of 6 times of volumes of impouring, extracted in soxhlet's extractor 72 hours with dehydrated alcohol behind the sedimentation and filtration then, and vacuum lyophilization promptly obtains the lower molecular weight cm-chitosan that 2-hydroxyl-5-oil of mirbane methyl replaces.
This compound is identified with infrared spectra, at 1643.08cm
-1The place is the absorption peak of secondary amine formation vibration, and 1461.90 is the skeleton stretching vibration of phenyl ring, and 1512.25 is the characteristic absorbance of the asymmetrical stretching vibration of nitro, proves the formation of target product.
Claims (8)
1, a kind of method for preparing general formula (I) compound
Y represents an active group in the formula
This method comprises following key step:
(1). the substituted salicylic aldehydes reaction of cm-chitosan and general formula (II) is obtained the schiff bases intermediate;
Formula (II)
(2). use NaBH
4Reduction makes general formula (I) compound;
(3). obtain throw out in the reaction product impouring organic solvent;
(4). after filtration, separate,, obtain the N-substituted carboxymethyl chitosan of formula (I) with alcoholic solvent purification by liquid extraction in cable type extractor according.
2, according to the described method of claim 1, wherein Y represents a chlorine atom or nitro.
3, according to the described method of claim 1, it is characterized in that cm-chitosan and substituted salicylic aldehydes react in the aqueous solution, the mol ratio of cm-chitosan and substituted salicylic aldehydes is 1: 3-1: 5, the reaction times is 1-3 hour.
4, according to the described method of claim 1, it is characterized in that used substituted salicylic aldehydes and NaBH
4Mol ratio be 1: 1.5-1: 3, the reaction times is 2-4 hour.
5, according to the described method of claim 1, said cm-chitosan is characterized in that the molecular weight of chitosan wherein between 1-70 ten thousand, and deacetylation is 80-100%.
6, according to the described method of claim 1, it is characterized in that being used for sedimentary organic solvent volume the 3-6 that is the liquor capacity total amount doubly, said organic solvent is selected from acetone or 80% above ethanol; The alcoholic solvent that is used for purification by liquid extraction is a dehydrated alcohol.
7, the N-2-hydroxyl that obtains according to the described preparation method of claim 1-5-chlorophenylmethyl cm-chitosan, its structural formula is:
Wherein Fan Ying amino of chitosan group does not comprise by methylol replacing part, accounts for the 34.3-56.5% of amino total amount in the chitosan; Its characteristic infrared spectrum (cm
-1) 3468.86,2924.61,1654.62,1614.44,1465.15,1004.90,866.00,722.64.
8, according to the described preparation method of claim 1, the N-2-that obtains hydroxyl-5-oil of mirbane methyl cm-chitosan, its structural formula is:
Wherein Fan Ying amino of chitosan group does not comprise by methylol replacing part, accounts for the 34.3-56.5% of amino total amount in the chitosan; Its characteristic infrared spectrum (cm
-1): 3516.48,1643.08,1512.25,1464.90,871.12,697.27.
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Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101157734B (en) * | 2007-09-07 | 2010-06-16 | 中国科学院海洋研究所 | Chitosan alpha-aminoalkyl phosphonate ester derivative and preparation method thereof |
| CN101518258B (en) * | 2009-04-10 | 2012-06-06 | 暨南大学 | Method for preparing matrine/carboxymethyl chitosan/phosphonic chitosan pesticide nanoparticle aqueous dispersion preparation |
| CN101988202B (en) * | 2009-08-07 | 2013-05-22 | 中国科学院海洋研究所 | Carboxymethyl chitosan oligosaccharide schiff base organic carbon steel seawater corrosion inhibitor and application thereof |
| CN105801722A (en) * | 2016-03-28 | 2016-07-27 | 中国科学院海洋研究所 | Marine organism polysaccharide copper compound and preparation method and application thereof |
-
2005
- 2005-07-25 CN CNB2005100443072A patent/CN100497398C/en not_active Expired - Fee Related
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101157734B (en) * | 2007-09-07 | 2010-06-16 | 中国科学院海洋研究所 | Chitosan alpha-aminoalkyl phosphonate ester derivative and preparation method thereof |
| CN101518258B (en) * | 2009-04-10 | 2012-06-06 | 暨南大学 | Method for preparing matrine/carboxymethyl chitosan/phosphonic chitosan pesticide nanoparticle aqueous dispersion preparation |
| CN101988202B (en) * | 2009-08-07 | 2013-05-22 | 中国科学院海洋研究所 | Carboxymethyl chitosan oligosaccharide schiff base organic carbon steel seawater corrosion inhibitor and application thereof |
| CN105801722A (en) * | 2016-03-28 | 2016-07-27 | 中国科学院海洋研究所 | Marine organism polysaccharide copper compound and preparation method and application thereof |
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