CN1478777A - Method of preparing 2,4,6-triisopropanyl-1,3,5-trioxy oxane - Google Patents
Method of preparing 2,4,6-triisopropanyl-1,3,5-trioxy oxane Download PDFInfo
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- CN1478777A CN1478777A CNA031168779A CN03116877A CN1478777A CN 1478777 A CN1478777 A CN 1478777A CN A031168779 A CNA031168779 A CN A031168779A CN 03116877 A CN03116877 A CN 03116877A CN 1478777 A CN1478777 A CN 1478777A
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- chloride
- triisopropyl
- trioxane
- ionic liquid
- isobutyric aldehyde
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Abstract
A process for preparing 2,4,6-triisopropyl-1,3,5-trioxyoxane includes such steps as cyclizing tripolymerizing reaction of ionic liquid chosen from triethylamine aluminium chloride hydrochloride, triethylamin iron chloride hydrochloride, etc on isobutanal to obtain coarse product, filter, recrystallizing in absolute alcohol and vacuum drying. Its advantages are high purity (99%), high output rate, and cyclic use of catalyst.
Description
Technical field
The present invention relates to a kind of preparation 2,4,6-triisopropyl-1,3, the method for 5-trioxane, exactly, relating to the ionic liquid is Preparation of Catalyst 2,4,6-triisopropyl-1,3, the method for 5-trioxane belongs to the organic chemistry synthesis technical field.
Background technology
2,4,6-triisopropyl-1,3,5-trioxane be as a kind of broad-spectrum daily fine chemical product, is a kind of nontoxic, odorless, white crystal with good distillation performance.Its compound can be widely used as anti-mould and anti-moth goods, air freshener, health reodorant of knitted fabric and textile, leather, paper, file books etc., it is the ideal substitute of traditional naphthalene and santochlor, be applicable to places such as family, hotel, Library, also can be widely used as the intermediate of grain mould inhibitor, pesticide slow-releasing agent, medicine and dyestuff etc.
Traditional preparation method is to be raw material with the isobutyric aldehyde, with inorganic acid as catalyst, carries out cyclic trimerization reaction and aftertreatment, obtains 2,4,6-triisopropyl-1,3,5-trioxane.As German Patent Ger.offen.2,424,128 adopt H
2SO
4, HCl, H
3PO
4Deng making catalyzer, Japanese Patent 78101386 adopts ZrO
2, ZrO (OH)
2, Zr (OH)
4, TiO
2Or SnO
2Make catalyzer.But adopt H
2SO
4, HCl, H
3PO
4Etc. liquid acid during as catalyzer, problem such as have that long reaction time, product yield are low, environmental pollution and equipment corrosion are serious is as adopting H
2SO
4During as catalyzer, though the reaction times reaches 9 hours, isobutyric aldehyde still can not be realized transforming fully, and product yield is low, is 87.5%.Adopt ZrO
2, ZrO (OH)
2, Zr (OH)
4, TiO
2Or SnO
2During as catalyzer, there are problems such as long reaction time, transformation efficiency is low, catalyzer costs an arm and a leg Deng solid acid, as adopting ZrO
2During as catalyzer, though the reaction times reaches 12 hours, isobutyric aldehyde still can not be realized transforming fully, and product yield has only 80%.Chinese patent CN1061597A has reported heteropolyacids such as employing phospho-molybdic acid, phospho-wolframic acid as catalyzer recently, can make isobutyric aldehyde carry out the cyclic trimerization reaction, obtains 2,4,6-triisopropyl-1,3,5-trioxane.Though this method product yield height is 97.2%, the catalyzer costliness can not recycle again, when removing catalyzer with diluted alkaline and water elution in addition, can produce a large amount of waste water, causes serious environmental to pollute.Therefore, background technology can't realize yield height, low, the eco-friendly target of cost simultaneously.
Summary of the invention
Ionic liquid is as a kind of eco-friendly new catalytic material, is one of research focus in the emerging in recent years Green Chemistry.It generally is made of inorganic anion and organic cation.With the ionic liquid is Preparation of Catalyst 2,4, and 6-triisopropyl-1,3,5-trioxane are the effective ways that solves the existing problem of background technology.
The problem to be solved in the present invention provides a kind of preparation 2,4,6-triisopropyl-1,3, the method for 5-trioxane, this method have the reaction times short, transformation efficiency is high, yield is high, environmental friendliness, the advantage little to equipment corrosion.
The present invention solves this technical problem by the following technical programs.It is characterized in that isobutyric aldehyde carries out the cyclic trimerization reaction under the condition that with one of ionic liquid Triethylammonium chloride aluminum chloride, Triethylammonium chloride iron(ic) chloride, 1-butyl-3-Methylimidazole aluminum chloride and 1-butyl-3-Methylimidazole iron(ic) chloride is catalyzer, obtain 2,4,6-triisopropyl-1,3, the thick product of 5-trioxane, thick product is through suction filtration, recrystallization, vacuum-drying, obtain purity 2,4 more than 99.0%, 6-triisopropyl-1,3, the highly finished product of 5-trioxane.
Now describe technical scheme of the present invention in detail.According to above-described preparation 2,4,6-triisopropyl-1,3, the method for 5-trioxane is characterized in that, operation steps:
The cyclic trimerization reaction of the 1st step
In there-necked flask, add the isobutyric aldehyde of 24 parts of weight and the ionic liquid of 0.5～2 part of weight, ionic liquid is one of Triethylammonium chloride aluminum chloride, Triethylammonium chloride iron(ic) chloride, 1-butyl-3-Methylimidazole aluminum chloride and 1-butyl-3-Methylimidazole iron(ic) chloride, under normal pressure, nitrogen protection, 10～50 ℃ of temperature of reaction and stirring condition, reacted 0.5～3 hour, and be cooled to room temperature, in reaction process, the isobutyric aldehyde liquid phase reduces gradually, and white crystals is separated out gradually;
The 2nd step suction filtration
Adopt method of pumping filtration that white crystals is separated with ionic liquid and unreacted isobutyric aldehyde, obtain 2,4,6-triisopropyl-1,3, the thick product of 5-trioxane, yield reaches 66.8～97.6%;
The 3rd step recrystallization and vacuum-drying
The thick product in last step is mixed with dehydrated alcohol, the dehydrated alcohol consumption is: dehydrated alcohol/thick product=0.5～5/1 (wt/wt), with mixture heating up to 50 ℃, become homogeneous phase, slowly cool to room temperature again, separate out white crystals,, obtain the highly finished product of purity more than 99.0% again through suction filtration, absolute ethanol washing, vacuum-drying;
The 4th ion liquid repeated use of step
The 1st step that ionic liquid and unreacted isobutyric aldehyde one are used from preparation next time will be obtained in the 2nd step.
The chemical reaction relevant with above-mentioned preparation method is expressed as with skeleton symbol:
Compare with background technology, the present invention has following tangible advantage:
1, the reaction times is short.
2, the yield height reaches as high as 97.6%.
3, little to equipment corrosion.
4, environmental friendliness can realize that cleaning is green synthetic.
5, catalyzer and unreacted raw material can be recycled and reused for preparation next time.
Embodiment
All embodiment operate according to operation steps of the present invention fully.
Embodiment 1
The 1st step
Isobutyric aldehyde 24.0g, ionic liquid are Triethylammonium chloride aluminum chloride, and add-on is 2.0g, and temperature of reaction is 25 ℃, react 1 hour;
The 2nd step
Yield is 94.0%.
Embodiment 2
Except for the following differences, all the other and embodiment 1 are identical: the 1st step intermediate ion liquid add-on is 1.0g, and yield is 93.4% in the 2nd step.
Embodiment 3
Except for the following differences, all the other and embodiment 1 are identical: the 1st step intermediate ion liquid add-on is 1.0g, and temperature of reaction is 10 ℃, and yield is 94.1% in the 2nd step.
Embodiment 4
Except for the following differences, all the other and embodiment 1 are identical: the 1st step intermediate ion liquid add-on is 1.0g, and temperature of reaction is 50 ℃, and yield is 66.8% in the 2nd step.
Embodiment 5
Except for the following differences, all the other and embodiment 1 are identical: the 1st step intermediate ion liquid add-on is 0.5g, and temperature of reaction is 10 ℃, and yield is 69.2% in the 2nd step.
Embodiment 6
Except for the following differences, all the other and embodiment 1 are identical: the 1st step intermediate ion liquid is 1-butyl-3-Methylimidazole aluminum chloride, and add-on is 2.0g, and yield is 92.1% in the 2nd step.
Embodiment 7
The 1st step
Isobutyric aldehyde 24.0g, ionic liquid are Triethylammonium chloride iron(ic) chloride, and add-on is 2.0g, and temperature of reaction is 25 ℃, react 1 hour.
The 2nd step
Yield is 97.6%.
Embodiment 8
Except for the following differences, all the other and embodiment 7 are identical: the 1st step intermediate ion liquid add-on is 1.0g, and yield is 96.0% in the 2nd step.
Embodiment 9
Except for the following differences, all the other and embodiment 7 are identical: the 1st step intermediate ion liquid add-on is 0.5g, and yield is 67.1% in the 2nd step.
Embodiment 10
Except for the following differences, all the other and embodiment 7 are identical: the 1st step intermediate ion liquid is 1-butyl-3-Methylimidazole iron(ic) chloride, and add-on is 2.0g, and yield is 94.1% in the 2nd step.
Claims (2)
1. one kind prepares 2,4,6-triisopropyl-1,3, the method for 5-trioxane is characterized in that, isobutyric aldehyde carries out the cyclic trimerization reaction under the condition that with one of ionic liquid Triethylammonium chloride aluminum chloride, Triethylammonium chloride iron(ic) chloride, 1-butyl-3-Methylimidazole aluminum chloride and 1-butyl-3-Methylimidazole iron(ic) chloride is catalyzer, obtain 2,4,6-triisopropyl-1,3, the thick product of 5-trioxane, thick product obtains purity 2 more than 99.0% through suction filtration, recrystallization, vacuum-drying, 4,6-triisopropyl-1,3, the highly finished product of 5-trioxane.
2. preparation 2,4 according to claim 1,6-triisopropyl-1,3, the method for 5-trioxane is characterized in that, operation steps:
The cyclic trimerization reaction of the 1st step
In there-necked flask, add the isobutyric aldehyde of 24 parts of weight and the ionic liquid of 0.5～2 part of weight, ionic liquid is one of Triethylammonium chloride aluminum chloride, Triethylammonium chloride iron(ic) chloride, 1-butyl-3-Methylimidazole aluminum chloride and 1-butyl-3-Methylimidazole iron(ic) chloride, under normal pressure, nitrogen protection, 10～50 ℃ of temperature of reaction and stirring condition, reacted 0.5～3 hour, and be cooled to room temperature, in reaction process, the isobutyric aldehyde liquid phase reduces gradually, and white crystals is separated out gradually;
The 2nd step suction filtration
Adopt method of pumping filtration that white crystals is separated with ionic liquid and unreacted isobutyric aldehyde, obtain 2,4,6-triisopropyl-1,3, the thick product of 5-trioxane, yield reaches 66.8～97.6%;
The 3rd step recrystallization and vacuum-drying
The thick product in last step is mixed with dehydrated alcohol, the dehydrated alcohol consumption is: dehydrated alcohol/thick product=0.5～5/1 (wt/wt), with mixture heating up to 50 ℃, become homogeneous phase, slowly cool to room temperature again, separate out white crystals,, obtain the highly finished product of purity more than 99.0% again through suction filtration, absolute ethanol washing, vacuum-drying;
The 4th ion liquid repeated use of step
The 1st step that ionic liquid and unreacted isobutyric aldehyde one are used from preparation next time will be obtained in the 2nd step.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 03116877 CN1211380C (en) | 2003-05-13 | 2003-05-13 | Method of preparing 2,4,6-triisopropanyl-1,3,5-trioxy oxane |
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 03116877 CN1211380C (en) | 2003-05-13 | 2003-05-13 | Method of preparing 2,4,6-triisopropanyl-1,3,5-trioxy oxane |
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| Publication Number | Publication Date |
|---|---|
| CN1478777A true CN1478777A (en) | 2004-03-03 |
| CN1211380C CN1211380C (en) | 2005-07-20 |
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Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN100372842C (en) * | 2006-05-19 | 2008-03-05 | 华东师范大学 | Method for preparing 2,4-diiso propyl-5,5-dimethyl-1,3-dioxane |
| CN109794296A (en) * | 2018-12-29 | 2019-05-24 | 濮阳宏业高新科技发展有限公司 | A kind of mixed acid solid-carried catalyst and the application in catalysis n-butanal or the reaction of isobutylaldehyde cyclic trimerization |
| CN110357849A (en) * | 2019-07-29 | 2019-10-22 | 润泰化学股份有限公司 | A method of preparing three oxygen oxane of 2,4,6- triisopropyl -1,3,5- |
-
2003
- 2003-05-13 CN CN 03116877 patent/CN1211380C/en not_active Expired - Fee Related
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN100372842C (en) * | 2006-05-19 | 2008-03-05 | 华东师范大学 | Method for preparing 2,4-diiso propyl-5,5-dimethyl-1,3-dioxane |
| CN109794296A (en) * | 2018-12-29 | 2019-05-24 | 濮阳宏业高新科技发展有限公司 | A kind of mixed acid solid-carried catalyst and the application in catalysis n-butanal or the reaction of isobutylaldehyde cyclic trimerization |
| CN110357849A (en) * | 2019-07-29 | 2019-10-22 | 润泰化学股份有限公司 | A method of preparing three oxygen oxane of 2,4,6- triisopropyl -1,3,5- |
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| Publication number | Publication date |
|---|---|
| CN1211380C (en) | 2005-07-20 |
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