CN107955822A - A kind of lipase-catalyzed online synthesis S-（4- methyl-benzyls）The method of laurate thioesters - Google Patents
A kind of lipase-catalyzed online synthesis S-（4- methyl-benzyls）The method of laurate thioesters Download PDFInfo
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Abstract
The invention discloses a kind of method of lipase-catalyzed online synthesis S (4 methyl-benzyl) laurate thioesters：Using dimethyl sulfoxide as reaction dissolvent, using molar ratio as 1:0.5~6 4 methyl benzyl mercaptans and vinyl laurate are raw material; using Lipozyme TL IM as catalyst; raw material and reaction dissolvent are placed in syringe; Lipozyme TL IM are uniformly filled in the reaction channel of microfluidic channel reactor; raw material and reaction dissolvent is continuously passed through in reaction channel device under the promotion of syringe pump and carry out acylation reaction; the reaction channel internal diameter of the microfluidic channel reactor is 0.8~2.4mm, a length of 0.5~1.0m of reaction channel；It is 20~60 DEG C to control acylation reaction temperature, and the acylation reaction time is 20~40min, collects reaction solution online by product collector, reaction solution obtains S (4 methyl-benzyl) laurate thioesters through conventional post processing.The present invention has the advantages that short reaction time, high selectivity and yield are high.
Description
(1) technical field
The present invention relates to a kind of method of lipase-catalyzed online synthesis S- (4- methyl-benzyls) laurate thioesters.
(2) background technology
Many artificial synthesized or natural organic compounds containing sulfur all has bioactivity.Sulfur ester is unique because of it
Chemical constitution and with anti-oxidant, antibacterial, the pharmacological activity such as antitumor, be in important in organic synthesis and chemical biology
Mesosome.Meanwhile thioesters class formation also has the function that to protect unstable thiol functionalities, increases its pharmaceutical activity, covers SH
The smell of key, in food, medicine, pesticide and cosmetic industry extensive use.
The synthesis of sulfur ester generally uses esterification process, and this method is mainly using strong acid such as sulfuric acid, benzene sulfonic acids as urging
Agent, this kind of catalytic erosion is strong, harsh to equipment requirement, and environmental pollution is serious.Separately have been reported that using fluoroform sulphonate
Or it is transition metal-catalyzed prepare sulfur ester, this kind of reaction prepares difficult, expensive, easy there are transition metal complex
Loss, more difficult recycling, can produce the shortcomings of environmentally harmful material.With becoming increasingly conspicuous for problem of environmental pollution, compel highly necessary
The green high-efficient synthetic method for seeking development less to human health and environmental hazard.
Enzymic catalytic reaction is an emphasis of Green Chemistry research.Enzymatic reaction is because its reaction condition is gentle, high selectivity
And substrate specificity scope extensively causes extensive concern in organic synthesis.But enzymatic reaction is when generally requiring longer reaction
Between, and for specific substrates there are the restriction that reaction medium suppresses substrate dissolving with enzyme activity, thus in biocatalytic reaction
On the basis of develop a kind of enzymatic sulfur ester based on micro-fluidic reaction technology become our research hotspot.
Microflow control technique a special kind of skill emerging since being 20th century 90, be it is a kind of be empty as the scale of the order of magnitude using micron
Between to reactant carry out manipulation for main feature technology, can be by the operating unit collection such as the preparation of sample, reaction, separation, detection
Into on one piece of small chip, network is formed by microchannel, whole system is run through with controlled fluid, so as to substitute routine biochemistry
The multiple functions in laboratory.Microflow control technique is widely used in fields such as biology, chemistry and medicine.
Nineteen ninety-five, micro-system are applied to chemistry and biology in WESTERN GERMANY Mainz laboratory first
Reaction, this can regard the micro-system widely applied beginning as.The first international conference on microtechnology is held within 1997
(IMRET1).So far, micro-fluidic chip reactor has been successfully used to a variety of organic synthesis, and illustrates and be widely applied
Prospect.With the development of microring array, micro-reacting tcchnology in micro-fluidic chip, synthetic reaction is carried out in the chips and has become miniflow
Control one of research hotspot of chip field.
Compared with conventional chemical reactor, microchannel has the specific surface area of micron-sized internal diameter scale and super large, it
Diffusion length want it is short very much, mass transfer velocity is fast；Its heat transfer efficiency is also far above conventional chemical reactor, and it is acute to can be applied to reaction
Strong heat release or the reaction of high selectivity.The easy control of reaction conditions such as reactant ratio, temperature, reaction time and flow velocity, it is secondary anti-
Should be less；Need reactant dosage little, can not only reduce the dosage of expensive, poisonous adverse reaction thing, be produced in reaction process
Environmental contaminants it is also few, be a kind of environmental-friendly, study on the synthesis novel substance technology.
Up to the present, the research of Enzyme catalyzed synthesis sulfur ester is also relatively fewer, and enzymatic thioesters class chemical combination
The synthesis of thing uses acylase more, and this method needs the longer reaction time (48h) and for the conversion ratio of specific substrates reaction
It is not especially desirable, and reaction cost is higher.In order to develop a kind of efficient green, economic and environment-friendly sulfur ester synthesizes
New technology, we have studied the side of lipase-catalyzed online synthesis S- (4- methyl-benzyls) laurate thioesters in micro passage reaction
Method, it is intended to find a kind of new technology synthesized online of S- of high-efficiency environment friendly (4- methyl-benzyls) laurate thioesters.
(3) content of the invention
The technical problem to be solved in the present invention is to provide lipase-catalyzed online synthesis in a kind of microfluidic channel reactor
The new process of S- (4- methyl-benzyls) laurate thioesters, has the advantages that the reaction time is short, yield is high, selectivity is good.
In order to solve the above technical problems, the present invention adopts the following technical scheme that：
A kind of method of lipase-catalyzed online synthesis S- (4- methyl-benzyls) laurate thioesters, the method use miniflow
Channel reactor is controlled, the microfluidic channel reactor includes sequentially connected syringe, reaction channel and product collector,
The syringe is installed in syringe pump, and the syringe is connected by the first connecting pipe with reaction channel entrance, described
Product collector is connected by the second connecting pipe and reaction channel outlet, and the reaction channel internal diameter is 0.8~2.4mm, instead
Answer a length of 0.5~1.0m of passage；The described method includes：Using dimethyl sulfoxide as reaction dissolvent, with 4- methyl benzyl mercaptan and laurate
Vinyl acetate is raw material, and using Lipozyme TL IM as catalyst, the raw material and the reaction dissolvent are placed in
In syringe, Lipozyme TL IM are uniformly filled in reaction channel, are made under the promotion of syringe pump described
Raw material and the reaction dissolvent, which are continuously passed through in reaction channel, carries out acylation reaction, and controlling reaction temperature is 20~60 DEG C, instead
For 20~40min, (it is stagnant to reaction channel is left into reaction channel that the heretofore described reaction time refers to reactant between seasonable
The reaction time stayed), reaction solution is collected by product collector online, the reaction solution is post-treated to obtain S- (4- methyl
Benzyl) laurate thioesters；The ratio between the 4- methyl benzyl mercaptan and the amount of material of vinyl laurate are 1:0.5~6；It is described
The addition of catalyst 0.025~0.05g/mL is calculated as with the volume of reaction dissolvent used.
Further, in the microfluidic channel reactor that the present invention uses, the syringe number can be one or more,
Depending on specific reaction requirement.Reaction raw materials of the present invention are two kinds, preferably using two syringes, specifically, the injection
Device is the first syringe and the second syringe respectively, and first connecting pipe is Y types or T-shaped pipeline, first note
Emitter is connected to two interfaces of the Y types or T-shaped pipeline and by the Y types or T-shaped with the second note syringe
Pipeline is connected with the reaction channel, is increased by reactant molecule contact and the collision probability of microchannel, is made two bursts of reactions
Liquid stream is mixed and reacted in public reaction channel.
Further, more specifically, method of the present invention comprises the following steps：
The ratio between amount with material is 1:0.5~6 4- methyl benzyl mercaptan and vinyl laurate are raw material, with lipase
Lipozyme TL IM are catalyst, and using dimethyl sulfoxide as reaction dissolvent, Lipozyme TL IM are uniformly filled in
In reaction channel, first it is loaded on dimethyl sulfoxide dissolving 4- methyl benzyl mercaptan in the first syringe；Laurate is dissolved with dimethyl sulfoxide
Vinyl acetate is loaded in the second syringe；The first syringe, the second syringe are loaded in same syringe pump again, then in syringe pump
It is synchronous promote under make raw material and reaction dissolvent by the Y types or T-shaped pipeline collect and afterwards enter in reaction channel to carry out
Reaction, controlling reaction temperature are 20~60 DEG C, and the reaction time is 20~40min, and reaction solution is collected online by product collector,
Post-treated obtained S- (4- methyl-benzyls) the laurate thioesters of reaction solution；The addition of the catalyst is 0.5~1g.
The concentration of vinyl laurate is usually 0.05~0.6mmol/mL described in second syringe.
Heretofore described first syringe is consistent with the specification of the second syringe, 4- methyl benzyl described in the first syringe
The concentration of mercaptan is usually 0.1mmol/mL.
Further, the microfluidic channel reactor further includes insulating box, and the reaction channel is placed in insulating box,
Can effective controlling reaction temperature with this.The insulating box can voluntarily be selected according to reaction temperature requirement, for example water-bath is permanent
Incubator etc..
The present invention is unlimited for the material of reaction channel, it is recommended to use green, the material of environmental protection, such as silicone tube；For
The shape of reaction channel is preferably shaped form, it is ensured that reaction solution stably passes through.
In the present invention, the Lipozyme TL IM believe the business of (novozymes) company production using Novi
Product, it is a kind of by microorganism preparation, the system of 1,3 position-specifics, food-grade lipase (EC3.1.1.3) on particle silica gel
Agent.It is obtained from Thermomyceslanuginosus, with a kind of gene-modified aspergillus oryzae (Aspergillusoryzae)
Microorganism is by submerged fermentation production.
Lipozyme TLIM is uniformly filled in reaction channel by the method for the present invention, can directly will by Physical
Granular catalyst is uniformly fixed in reaction channel.
Further, the ratio between amount of material of the 4- methyl benzyl mercaptan and vinyl laurate is preferably 1:1~3, it is optimal
Elect 1 as:2.
Further, the acylation reaction temperature is preferably 45~55 DEG C, is most preferably 50 DEG C.
Further, the acylation reaction time is preferably 25~35min, is most preferably 30min.
The reaction product of the present invention can collect online, and gained reaction solution be able to can be obtained by conventional post-processing approach
S- (4- methyl-benzyls) laurate thioesters.It is described routine post-processing approach can be：The vacuum distillation of gained reaction solution removes solvent,
With 200-300 mesh silica gel wet method dress posts, elution reagent is petroleum ether:Ethyl acetate volume ratio=20:1, a small amount of elution of sample
Wet method upper prop after reagent dissolving, collects eluent, while TLC tracking elution processes, the elution containing single product that will be obtained
Liquid, which merges, to be evaporated, and can obtain yellow oily liquid, is S- (4- methyl-benzyls) laurate thioesters.
Compared with prior art, beneficial effects of the present invention are：
The present invention utilizes lipase-catalyzed online synthesis S- (4- methyl-benzyls) laurate in microfluidic channel reactor
Thioesters, which not only significantly shortens the reaction time, but also has high conversion ratio and selectivity；Utilize economy first at the same time
Lipozyme TL IM catalysis thioesters acylation reaction, reduce reaction cost, have economical and efficient advantage.
(4) illustrate
Fig. 1 is the structure diagram for the microfluidic channel reactor that the embodiment of the present invention uses.
In figure, 1,2- syringes, 3- reaction channels, 4- product collectors, 5- constant temperature water box.
(5) embodiment
Protection scope of the present invention is described further with specific embodiment below, but protection scope of the present invention is unlimited
In this：
The structural reference Fig. 1 for the microfluidic channel reactor that the embodiment of the present invention uses, including a syringe pump (are not shown
Show), two syringes 1 and 2, reaction channel 3, constant temperature water box (5, only show its floor map) and product collector 4；Two
A syringe 1 and 2 is installed in syringe pump, is connected by a Y types interface with 3 entrance of reaction channel, the reaction channel 3 is put
In constant temperature water box 5, by 5 controlling reaction temperature of constant temperature water box, the internal diameter 2.0mm of the reaction channel 3, pipe range
1m, the outlet of reaction channel 3 are connected by an interface with product collector 4.
Embodiment 1：The synthesis of S- (4- methyl-benzyls) laurate thioesters
Device is with reference to figure 1：4- methyl benzyl mercaptan (1.0mmol) is dissolved in 10mL DMSO, vinyl laurate
(2.0mmol) is dissolved in 10mL DMSO, is then loaded on respectively spare in 10mL syringes.0.87g Lipozymes
TL IM are uniformly filled in reaction channel, and under the promotion of 2000 syringe pumps of PHD, two-way reaction solution is respectively with 10.4 μ Lmin-1
Flow velocity by " Y " connector enter reaction channel in reacted, by constant temperature water box control temperature of reactor at 50 DEG C, instead
Liquid continuous flowing reactive 30min, reaction result in reaction channel is answered to pass through thin-layer chromatography TLC tracing detections.
Reaction solution is collected by product collector online, vacuum distillation removes solvent, is filled with 200-300 mesh silica gel wet method
Column, elution reagent are petroleum ether:Ethyl acetate volume ratio=20:1, pillar height 35cm, column diameter 4.5cm, a small amount of elution of sample
Wet method upper prop after reagent dissolving, eluent collect flow velocity 2mLmin-1, while TLC tracking elution processes, it will obtain containing single
The eluent of one product, which merges, to be evaporated, and obtains yellow oily liquid, obtains S- (4- methyl-benzyls) laurate thioesters, HPLC detections
4- methyl benzyl mercaptans conversion ratio 94%, selectivity 98%.
Nuclear-magnetism characterization result is as follows：
1H NMR(500MHz,CDCl3):δ=7.18 (d, J=7.6Hz, 2H), 7.12 (d, J=7.6Hz, 2H), 4.10
(s, 2H), 2.57 (s, 2H), 2.33 (s, 3H), 1.27 (s, 18H), 0.89 (d, J=7.1Hz, 3H)13C NMR(125MHz,
CDCl3):δ=199.1,137.0,134.7,129.4,128.8,43.9,32.9,32.0,29.7,29.6-2 9.2,29.0,
25.7,22.8,21.1,14.2.
Embodiment 2-5
It is subject to 4- methyl benzyl mercaptan dosages, changes 4- methyl benzyl mercaptan and laurate second in micro-fluidic micro passage reaction
The ratio between amount of substrate materials of enester, controls temperature 50 C, other are with embodiment 1, and the results are shown in Table 1：
Table 1:4- methyl benzyl mercaptan and the influence for comparing reaction of the amount of vinyl laurate substrate materials
| Embodiment | 4- methyl benzyl mercaptans:Vinyl laurate | Conversion ratio [%] | Selectivity [%] |
| 2 | 1:1 | 74 | 97 |
| 1 | 1:2 | 94 | 98 |
| 3 | 1:3 | 89 | 98 |
| 4 | 1:4 | 83 | 97 |
| 5 | 1:5 | 80 | 96 |
Table 1 the result shows that, when flow velocity is 10.4 μ Lmin-1, the reaction time is 30min, and reaction temperature is 50
DEG C, reactor is using DMSO as organic solvent, and with the increase of reactant vinyl laurate, the conversion ratio of reaction is also with increasing
Add, when substrate than 4- methyl benzyl mercaptan and vinyl laurate is 1:When 2, the conversion ratio of reaction is optimal, so micro- in the present invention
The ratio between amount of optimal substrate materials is 1 in flow control micro passage reaction:2.
Embodiment 6-9
Change the temperature of microfluidic channel reactor, with embodiment 1, reaction result is as shown in table 2 for other：
Table 2：Influence of the temperature to reaction
| Embodiment | Temperature [DEG C] | Conversion ratio [%] | Selectivity [%] |
| 6 | 40 | 73 | 95 |
| 7 | 45 | 86 | 97 |
| 1 | 50 | 94 | 98 |
| 8 | 55 | 88 | 96 |
| 9 | 60 | 85 | 95 |
Table 2 the result shows that, when flow velocity is 10.4 μ Lmin-1, the reaction time is 30min, and reactor is using DMSO to have
The ratio between amount of solvent, reactant 4- methyl benzyl mercaptan and vinyl laurate material is 1:2, when reaction temperature is in 50 DEG C
When, the conversion ratio of reaction is optimal, temperature or the Tai Gao or too low activity that will all influence enzyme.So micro-fluidic microchannel in the present invention
Optimum temperature is 50 DEG C in reactor.
Embodiment 10-13
Change the reaction time of microfluidic channel reactor, with embodiment 1, reaction result is as shown in table 3 for other：
Table 3：Influence of the reaction time to reaction
| Embodiment | Time [DEG C] | Conversion ratio [%] | Selectivity [%] |
| 10 | 20 | 78 | 95 |
| 11 | 25 | 87 | 96 |
| 1 | 30 | 94 | 98 |
| 12 | 35 | 90 | 99 |
| 13 | 40 | 84 | 96 |
Table 3 the result shows that, when reactor is using DMSO as organic solvent, reactant 4- methyl benzyl mercaptan and vinyl laurate
The ratio between amount of ester material is 1:2, reaction temperature is 50 DEG C, when reacted between when be 30min, reaction conversion ratio is up to
94%.So optimum reacting time 30min in micro-fluidic micro passage reaction in the present invention.
Comparative example 1-3
Change the catalyst in micro-fluidic micro passage reaction, be changed to porcine pancreatic lipase PPL (comparative example 1), fat respectively
Enzyme Novozym 435 (comparative example 2), bacillus alkaline protease (comparative example 3), other are with embodiment 1, as a result such as the institute of table 4
Show.
Table 4：Influence of the different enzymes to reaction conversion ratio and selectivity
| Comparative example | Enzyme source | Conversion ratio [%] | Selectivity [%] |
| 1 | PPL | 25 | 79 |
| 2 | Novozym 435 | 15 | 96 |
| 3 | Bacillus alkaline protease | 27 | 82 |
| Embodiment 1 | Lipozyme TL IM | 94 | 98 |
Table 4 the result shows that, for the acylation reaction of enzymatic 4- methyl benzyl mercaptans in microfluidic channel reactor, no
Same enzyme has fairly obvious influence to reaction.Utilize bacillus alkaline protease catalytic reaction, S- (4- methyl-benzyls)
The conversion ratio of laurate thioesters is 27%.And it is catalyzed the reaction, S- (4- methyl-benzyls) laurate thioesters using Novozym 435
Conversion ratio be only 15%.In terms of the result of table 4, the acylation for enzymatic 4- methyl benzyl mercaptans in microfluidic channel reactor is anti-
For answering, most effective catalyst is that the conversion ratio of Lipozyme TL IM, 4- methyl benzyl mercaptans is 94%, selectivity
For 98%.
Claims (9)
- A kind of 1. method of lipase-catalyzed online synthesis S- (4- methyl-benzyls) laurate thioesters, it is characterised in that：The side Method uses microfluidic channel reactor, the microfluidic channel reactor include sequentially connected syringe, reaction channel and Product collector, the syringe are installed in syringe pump, and the syringe is entered by the first connecting pipe with reaction channel Mouth connection, the product collector are connected by the second connecting pipe and reaction channel outlet, and the reaction channel internal diameter is 0.8 ~2.4mm, a length of 0.5~1.0m of reaction channel；The described method includes：Using dimethyl sulfoxide as reaction dissolvent, with 4- methyl benzyl sulphur Alcohol and vinyl laurate are raw material, using Lipozyme TL IM as catalyst, by the raw material and described anti- Answer solvent to be placed in syringe, Lipozyme TL IM are uniformly filled in reaction channel, in the promotion of syringe pump Under the raw material and the reaction dissolvent is continuously passed through in reaction channel and is carried out acylation reaction, controlling reaction temperature 20 ~60 DEG C, the reaction time is 20~40min, collects reaction solution online by product collector, the reaction solution is post-treated Obtain S- (4- methyl-benzyls) laurate thioesters；The ratio between the 4- methyl benzyl mercaptan and the amount of material of vinyl laurate are 1:0.5~6；The addition of the catalyst is calculated as 0.025~0.05g/mL with the volume of reaction dissolvent used.
- 2. the method for lipase-catalyzed online synthesis S- (4- methyl-benzyls) laurate thioesters as claimed in claim 1, it is special Sign is：The syringe has two, is the first syringe and the second syringe respectively, and first connecting pipe is Y Type or T-shaped pipeline, first syringe and the second note syringe are connected to two of the Y types or T-shaped pipeline Interface is simultaneously connected by the Y types or T-shaped pipeline with the reaction channel.
- 3. the method for lipase-catalyzed online synthesis S- (4- methyl-benzyls) laurate thioesters as claimed in claim 2, it is special Sign is：The method comprises the following steps：The ratio between amount with material is 1:0.5~6 4- methyl benzyl mercaptan and laurate Vinyl acetate is raw material, using Lipozyme TL IM as catalyst, using dimethyl sulfoxide as reaction dissolvent, by lipase Lipozyme TL IM are uniformly filled in reaction channel, are first loaded on the first syringe with dimethyl sulfoxide dissolving 4- methyl benzyl mercaptan In；It is loaded on dimethyl sulfoxide dissolving vinyl laurate in the second syringe；Again by the first syringe, the second syringe loaded on same In one syringe pump, then raw material and reaction dissolvent is set to collect by the Y types or T-shaped pipeline under the synchronous promotion of syringe pump And enter in reaction channel reacted afterwards, controlling reaction temperature is 20~60 DEG C, and the reaction time is 20~40min, passes through production Thing collector collects reaction solution, post-treated obtained S- (4- methyl-benzyls) the laurate thioesters of reaction solution online；The catalysis The addition of agent is calculated as 0.5~1g with the volume of reaction dissolvent used.
- 4. the method for lipase-catalyzed online synthesis S- (4- methyl-benzyls) laurate thioesters as claimed in claim 1, it is special Sign is：The microfluidic channel reactor includes insulating box, and the reaction channel is placed in insulating box.
- 5. the method for lipase-catalyzed online synthesis S- (4- methyl-benzyls) laurate thioesters as claimed in claim 3, it is special Sign is：The microfluidic channel reactor includes insulating box, and the reaction channel is placed in insulating box.
- 6. the side of lipase-catalyzed online synthesis S- (4- methyl-benzyls) laurate thioesters as described in one of Claims 1 to 5 Method, it is characterised in that：The ratio between amount of material of the 4- methyl benzyl mercaptan and vinyl laurate is 1:1~3.
- 7. the side of lipase-catalyzed online synthesis S- (4- methyl-benzyls) laurate thioesters as described in one of Claims 1 to 5 Method, it is characterised in that：The acylation reaction temperature is 40~60 DEG C, and the acylation reaction time is 25~35min.
- 8. the side of lipase-catalyzed online synthesis S- (4- methyl-benzyls) laurate thioesters as described in one of Claims 1 to 5 Method, it is characterised in that：The ratio between amount of material of the 4- methyl benzyl mercaptan and vinyl laurate is 1:2.
- 9. the side of lipase-catalyzed online synthesis S- (4- methyl-benzyls) laurate thioesters as described in one of Claims 1 to 5 Method, it is characterised in that the post-processing approach is：The vacuum distillation of gained reaction solution removes solvent, gained crude on silica gel column layer Analysis separation, with 200-300 mesh silica gel wet method dress posts, elution reagent is petroleum ether:Ethyl acetate volume ratio 20:1 mixed solvent, Wet method upper prop after crude product is dissolved with a small amount of elution reagent, collects eluent, while TLC tracking elution processes, contains what is obtained The eluent for having single product, which merges, to be evaporated, and can obtain yellow oily liquid, is S- (4- methyl-benzyls) laurate thioesters.
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201711393233.2A CN107955822A (en) | 2017-12-21 | 2017-12-21 | A kind of lipase-catalyzed online synthesis S-（4- methyl-benzyls）The method of laurate thioesters |
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