CN1583768A - Preparation of N,N-di(2-ethoxyl) aminomethyl diethyl phosphoric acid - Google Patents
Preparation of N,N-di(2-ethoxyl) aminomethyl diethyl phosphoric acid Download PDFInfo
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- CN1583768A CN1583768A CN 200410046073 CN200410046073A CN1583768A CN 1583768 A CN1583768 A CN 1583768A CN 200410046073 CN200410046073 CN 200410046073 CN 200410046073 A CN200410046073 A CN 200410046073A CN 1583768 A CN1583768 A CN 1583768A
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- hydroxyethyl
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- aminomethyl diethyl
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Abstract
N, N-bis(2-hydroxyethyl) aminomethylphosphonic diethylester is concerned with preparation of aminomethylphosphonic diester. It includes: (1) reaction of formaldehyde water solution with diethanol; (2) decompression distilling to produce 3 - (2 -hydroxyethyl) - 1,3, - oxaazapentane; (3) adding anhydrous solid acid catalysts and phosphonous acid diester; (4) filtrating and recovering the catalysts to get yellow transparency products with yields of above 98% and 94%-94% contents of N, N-bis(2-hydroxyethyl) aminomethylphosphonic diethylester. It is prepared simply, and highly yields with more effective content. The product is reactive fire-retardant for environmental protection, capably used in plastics, especially in foamed polyamine ester.
Description
Technical field
The present invention is a kind of N, and two (2-hydroxyethyl) the aminomethyl diethyl phosphonate preparation methods of N-belong to aminomethyl diethyl phosphonate preparation field.
Background of invention
N, two (2-hydroxyethyl) the aminomethyl diethyl phosphonates (shown in the structural formula as I) of N-are a kind of non-halogen environment-friendly type reactive flame retardants, are mainly used in flame retardant of plastic, are particularly suitable for preparing urethane foam.U.S. Pat P3,076,010 discloses the detailed preparation method of this compound, and this synthetic method is that addition reaction generation intermediate water solution takes place for (1) diethanolamine and formaldehyde (37% the aqueous solution); (2) this intermediate water solution and diethyl phosphite reaction; (3) use extracted with diethyl ether; (4) underpressure distillation separate N, two (2-hydroxyethyl) the aminomethyl diethyl phosphonates of N-, the product yield is 95%, N in the product, the content of two (2-hydroxyethyl) the aminomethyl diethyl phosphonates of N-is 88%.Because the existence of water, phosphorous acid ester and product phosphonic acid ester are easy to hydrolysis under reaction conditions, also be easy to take place the ethyl substitution reaction on the nitrogen-atoms of diethanolamine simultaneously, even use poisonous and inflammable and explosive ether solvent extraction, also difficulty is separated by product from reaction system, uses this method to prepare N, and the yield of two (2-hydroxyethyl) the aminomethyl diethyl phosphonate products of N-is low, N in the product, the content of two (2-hydroxyethyl) the aminomethyl diethyl phosphonates of N-is not high.
Summary of the invention
N of the present invention, two (2-hydroxyethyl) the aminomethyl diethyl phosphonate preparation methods of N-, purpose is to improve the yield and the quality product of product.The objective of the invention is to realize as follows:
(1) add the formalin of 165 parts of (by weight, as follows) 37-40% in the reactor, stir and add in advance 206 parts of fused diethanolamine down, the maintenance temperature of reaction was reacted 0.5 to 1.5 hour at 30 to 50 ℃;
(2) underpressure distillation, pressure earlier 50 to 60 ℃ of distillations, continue underpressure distillation at 60 to 80 ℃ less than 0.095MPa then, steam moisture, obtain 3-(2-hydroxyethyl)-1, bad pentane of 3-oxygen azepine;
(3) 0.3-2.5 part anhydrous solid acid catalyst and 271 parts of diethyl phosphites are added 3-(2-hydroxyethyl)-1, the 3-oxazolidine, 20 ℃ under 80 ℃, reacted 1 to 6 hour, can add earlier 3-(2-hydroxyethyl)-1 to catalyzer, in the 3-oxazolidine, add diethyl phosphite then, also can add catalyzer in the diethyl phosphite earlier, add 3-(2-hydroxyethyl)-1 then, in the 3-oxazolidine, the anhydrous solid acid catalyst is a strong acid cation resin;
(4) reaction mass drops to room temperature, and filtering recovering catalyst gets light yellow or yellow transparent liquid product, and yield is more than 98%.
3-(2-hydroxyethyl)-1 is shown in the structural formula as I I of 3-oxazolidine.
The used anhydrous solid acid catalyst of the present invention can reclaim, and pollution-free to reaction mass.The catalyzer that reclaims need not carry out any processing or use diluted acid, as 5% hydrochloric acid, embathes 1 to 2 time, reuses still to have identical catalytic effect more than five times.
Infrared spectra and nuclear magnetic resonance spectrum detect proof, and the product principal constituent is N, two (2-hydroxyethyl) the aminomethyl diethyl phosphonates of N-, and N in the gas phase analysis proof product, the content of two (2-hydroxyethyl) the aminomethyl diethyl phosphonates of N-is 93% to 94%.The gas phase analysis condition is: chromatographic column is SPB-5, column length 30m, and post footpath 0.53mm, the thick 1.5nm of liquid film, persistently overheating to 140 ℃, stopped 4 minutes, with 10%/and being raised to 230 ℃, sensing chamber and gasification chambers temp are 285 ℃, hydrogen flame detector, solvent are chloroform.
N of the present invention, the preparation method is simple for two (2-hydroxyethyl) the aminomethyl diethyl phosphonates of N-, and the yield and the quality product of product all are significantly increased.Therefore, technical scheme of the present invention compared with prior art has outstanding substantive distinguishing features.
Purpose of the present invention, feature and advantage will be elaborated in conjunction with the embodiments.
Embodiment
Embodiment 1.
(1) adds 165 part 37% formalin in the reactor, be heated to 30 ℃, stir and add in advance 206 parts of fused diethanolamine in following 30 minutes.Adding the diethanolamine process is thermopositive reaction, keeps temperature of reaction at 30 ℃, reacts 1 hour.
(2) change reaction unit into underpressure distillation, under 50 ℃, pressure is less than 0.095MPa, and decompression steams water, continues underpressure distillation 2 hours down at 60 ℃ then.
(3) change back reaction unit with this water distilling apparatus, and cool to 40 ℃, add 0.8 part of anhydrous solid acid catalyst macroporous type strong acid cation resin, stir and in 1 hour, to add 271 parts of diethyl phosphites down, then in 50 ℃ of insulation reaction 2 hours.
(4) reaction mass drops to room temperature, and filtering recovering catalyst gets the yellow transparent liquid product, and yield is 99%.N in the gas phase analysis product, two (2-hydroxyethyl) the aminomethyl diethyl phosphonate content of N-are 94%.
Embodiment 2.(according to U.S. Pat P3,076,010 method)
(1) adds 24.4g 37% formalin in the reaction flask, stir down in 20 ℃ to 30 ℃ adding diethanolamine 30.9g.
(2) add the 41.4g diethyl phosphite in 20 ℃ to 30 ℃.Owing to be thermopositive reaction, guarantee that temperature of reaction maintains 35 ℃ under the cooling, cool to 30 ℃ in about 40 minutes, and continue to stir for some time in room temperature, be heated to 50 ℃ of reactions 15 minutes then.
(3),, divide water-yielding stratum with 100ml extracted with diethyl ether reactant with the reactant cooling.
(4) underpressure distillation concentrates water layer, and the cut of 50 ℃/1mmHg is collected in underpressure distillation then, obtains product, yield 94.8%.N in the gas phase analysis product, two (2-hydroxyethyl) the aminomethyl diethyl phosphonate content of N-are 88%.
Embodiment 3.
As different from Example 1:
The formalin of adding 40% in step (1) reactor keeps temperature of reaction at 40 ℃, reacts 1.5 hours.
Step (2) changes reaction unit into underpressure distillation, and under 60 ℃, pressure is less than 0.095MPa, and decompression steams water, continues underpressure distillation 2 hours down at 80 ℃ then.
Step (3) cools to 50 ℃, adds 1.3 parts of anhydrous solid acid catalysts.Then in 40 ℃ of insulation reaction 3 hours
Get the yellow transparent liquid product, yield is 99%.N in the gas phase analysis product, two (2-hydroxyethyl) the aminomethyl diethyl phosphonate content of N-are 94%.
Embodiment 4.
As different from Example 1:
Step (1) keeps temperature of reaction at 50 ℃, reacts 1.5 hours.
Step (3) cools to 55 ℃, adds 0.4 part of anhydrous solid acid catalyst.Then in 55 ℃ of insulation reaction 4 hours
Get the yellow transparent liquid product, yield is 99%.N in the gas phase analysis product, two (2-hydroxyethyl) the aminomethyl diethyl phosphonate content of N-are 94%.
Embodiment 5.
As different from Example 1:
Step (3) adds 1.0 parts of anhydrous solid acid catalysts.Then in 80 ℃ of insulation reaction 1 hour
Get the yellow transparent liquid product, yield is 98%.N in the gas phase analysis product, two (2-hydroxyethyl) the aminomethyl diethyl phosphonate content of N-are 93%.
Embodiment 6.
As different from Example 1:
Step (3) adds 1.0 parts of anhydrous solid acid catalysts.Then in 20 ℃ of insulation reaction 6 hours
Get the yellow transparent liquid product, yield is 98%.N in the gas phase analysis product, two (2-hydroxyethyl) the aminomethyl diethyl phosphonate content of N-are 93%.
Embodiment 7.
As different from Example 1:
Step (3) adds 1.0 parts and reclaims and reuse five times anhydrous solid acid catalyst, then in 45 ℃ of insulation reaction 4 hours.
Get the yellow transparent liquid product, yield is 99%.N in the gas phase analysis product, two (2-hydroxyethyl) the aminomethyl diethyl phosphonate content of N-are 94%.
Claims (6)
1. N, the preparation method of two (2-hydroxyethyl) the aminomethyl diethyl phosphonates of N-may further comprise the steps:
(1) add the formalin of 165 parts of (by weight, as follows) 37-40% in the reactor, stir and add in advance 206 parts of fused diethanolamine down, the maintenance temperature of reaction was reacted 0.5-1.5 hour at 30 to 50 ℃;
(2) underpressure distillation steams moisture, obtains 3-(2-hydroxyethyl)-1, the 3-oxazolidine;
(3) 0.3 to 2.5 part of anhydrous solid acid catalyst and 271 parts of diethyl phosphites are added 3-(2-hydroxyethyl)-1, the 3-oxazolidine, 20 ℃ under 80 ℃, reacted 1 to 6 hour;
(4) reaction mass drops to room temperature, and filtering recovering catalyst gets the yellow transparent liquid product.
2. N according to claim 1, the preparation method of two (2-hydroxyethyl) the aminomethyl diethyl phosphonates of N-is characterized in that underpressure distillation in the step (2), pressure earlier 50 to 60 ℃ of distillations, continues underpressure distillation at 60 to 80 ℃ less than 0.095MPa then.
3. N according to claim 1, the preparation method of two (2-hydroxyethyl) the aminomethyl diethyl phosphonates of N-is characterized in that the anhydrous solid acid catalyst is a strong acid cation resin in the step (3).
4. according to claim 1 and 3 described N, the preparation method of two (2-hydroxyethyl) the aminomethyl diethyl phosphonates of N-is characterized in that anhydrous solid acid catalyst add-on is 0.4 to 1.3 part in the step (3).
5. according to claim 1 and 3 described N, the preparation method of two (2-hydroxyethyl) the aminomethyl diethyl phosphonates of N-is characterized in that the anhydrous solid acid catalyst is the catalyzer that last secondary response reclaims in the step (3).
6. according to claim 1 and 3 described N, the preparation method of two (2-hydroxyethyl) the aminomethyl diethyl phosphonates of N-, it is characterized in that in the step (3) 40 ℃ under 55 ℃, reacted 2-4 hour.
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| Application Number | Priority Date | Filing Date | Title |
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| CN 200410046073 CN1291992C (en) | 2004-06-04 | 2004-06-04 | Preparation of N,N-di(2-ethoxyl) aminomethyl diethyl phosphoric acid |
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| CN 200410046073 CN1291992C (en) | 2004-06-04 | 2004-06-04 | Preparation of N,N-di(2-ethoxyl) aminomethyl diethyl phosphoric acid |
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| CN1583768A true CN1583768A (en) | 2005-02-23 |
| CN1291992C CN1291992C (en) | 2006-12-27 |
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| CN 200410046073 Expired - Fee Related CN1291992C (en) | 2004-06-04 | 2004-06-04 | Preparation of N,N-di(2-ethoxyl) aminomethyl diethyl phosphoric acid |
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Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102276645A (en) * | 2011-05-18 | 2011-12-14 | 烟台万华聚氨酯股份有限公司 | Preparation method of diethyl N,N-bis(2- hydroxyethyl) aminomethylphosphonate |
| CN103435646A (en) * | 2013-08-21 | 2013-12-11 | 合肥安聚达新材料科技有限公司 | Phosphorous and nitrogenous UV-cured flame retardant and preparation method thereof |
| CN106519297A (en) * | 2016-11-11 | 2017-03-22 | 青岛科技大学 | Method for synthesizing flame retardant by aminolysis and phosphorous-nitrogen flame retardant |
| CN109651584A (en) * | 2018-11-20 | 2019-04-19 | 黎明化工研究设计院有限责任公司 | A kind of response type phosphate ester flame retardants and preparation method thereof and the application in polyurethane foam |
| CN112480362A (en) * | 2019-09-11 | 2021-03-12 | 广东广山新材料股份有限公司 | Polyurethane composition and preparation method and application thereof |
-
2004
- 2004-06-04 CN CN 200410046073 patent/CN1291992C/en not_active Expired - Fee Related
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102276645A (en) * | 2011-05-18 | 2011-12-14 | 烟台万华聚氨酯股份有限公司 | Preparation method of diethyl N,N-bis(2- hydroxyethyl) aminomethylphosphonate |
| CN102276645B (en) * | 2011-05-18 | 2014-04-16 | 万华化学集团股份有限公司 | Preparation method of diethyl N,N-bis(2- hydroxyethyl) aminomethylphosphonate |
| CN103435646A (en) * | 2013-08-21 | 2013-12-11 | 合肥安聚达新材料科技有限公司 | Phosphorous and nitrogenous UV-cured flame retardant and preparation method thereof |
| CN106519297A (en) * | 2016-11-11 | 2017-03-22 | 青岛科技大学 | Method for synthesizing flame retardant by aminolysis and phosphorous-nitrogen flame retardant |
| CN109651584A (en) * | 2018-11-20 | 2019-04-19 | 黎明化工研究设计院有限责任公司 | A kind of response type phosphate ester flame retardants and preparation method thereof and the application in polyurethane foam |
| CN109651584B (en) * | 2018-11-20 | 2021-10-08 | 黎明化工研究设计院有限责任公司 | Reactive phosphorus-containing flame retardant, preparation method thereof and application thereof in polyurethane foam |
| CN112480362A (en) * | 2019-09-11 | 2021-03-12 | 广东广山新材料股份有限公司 | Polyurethane composition and preparation method and application thereof |
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| Publication number | Publication date |
|---|---|
| CN1291992C (en) | 2006-12-27 |
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