CN1718569A - Method of preparing ethylenediamine tetracetonitrile and ethylenediamine tetraacetic acid using hydroxy acetonitrile as raw material - Google Patents
Method of preparing ethylenediamine tetracetonitrile and ethylenediamine tetraacetic acid using hydroxy acetonitrile as raw material Download PDFInfo
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- CN1718569A CN1718569A CN 200410069103 CN200410069103A CN1718569A CN 1718569 A CN1718569 A CN 1718569A CN 200410069103 CN200410069103 CN 200410069103 CN 200410069103 A CN200410069103 A CN 200410069103A CN 1718569 A CN1718569 A CN 1718569A
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- ethylenediamine
- acid
- hydroxyacetonitrile
- tetraacetic acid
- ethylene diamine
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Abstract
A process for preparing ethyldiamine tetraacetonitrile and ethyldiamine tetraacetic acid includes such steps as regulating the pH value of ethyldiamine solution to 6-8, adding hydroxyacetonitrile, reacting to obtain ethyldiamine diacetonitrile, heating to 60-100 deg.C, adding hydroxyaceto nitrile reacting to generate ethyldiamine tetraacetonitrile, cooling, filter, hydrolyzing in alkaline aqueous solution to obtain ethyldiamine tetraacetate, and adding acid to make pH=1-3 for obtaining ethyldiamine tetraacetic acid.
Description
Technical Field
The invention relates to a method for preparing ethylenediamine tetra-acetonitrile (EDTN), ethylenediamine tetra-acetic acid (EDTA) and salts by using hydroxy acetonitrile as a raw material.
Background
The Ethylene Diamine Tetraacetic Acid (EDTA) is a precursor of EDTA, and the EDTA can be obtained after acid hydrolysis or alkaline hydrolysis acidification. EDTA has a wide application range, is commonly used as a bleaching fixer in the processing of color photosensitive materials, and is also used as a dyeing auxiliary agent, a fiber processing auxiliary agent, a cosmetic additive, a masking agent for complexing and separating metal ions, a detergent, a stabilizer, a synthetic rubber polymerization initiator and the like. EDTA is a representative substance of chelating agents, and can form an extremely stable water-soluble complex with alkali metals, rare earth elements, transition metals and the like. In addition to sodium salts, there are amine salts and various salts of iron, magnesium, calcium, copper, manganese, zinc, cobalt, aluminum, etc., which have different uses.
CN 02133458.7 and US 5208363 describe the production of ethylenediamine tetraacetic nitrile in an acidic medium (pH 2-5.4) by using hydrocyanic acid, ethylenediamine and formaldehyde as raw materials, and because the gas hydrocyanic acid is used for gas-liquid reaction, potential safety and environmental protection hazards exist, and the equipment requirement is high.
CN98811975.7 and US6297397 describe the preparation of EDTA-Na by using ethylenediamine, NaCN and formaldehyde as raw materials under alkaline condition, and crystallizing by using methanol and other alcohol mixed solvent to obtain high-purity EDTA-Na.
GB871380, JP55151537 and the like describe the synthesis of EDTA by using high-purity liquid hydrocyanic acid, ethylenediamine and formaldehyde as raw materials, and the high-purity liquid hydrocyanic acid also has high cost, poor safety and the like. Shandong chemical engineering 1994(4), pages 24-25; zhejiang chemical industry 1988(6), pages 25-26, Guangzhou food industry science and technology 15(1), pages 15-46, 1999, introduces ethylenediamine, chloroacetic acid, sodium carbonate and the like as raw materials to prepare EDTA, because chloroacetic acid has no competitive power and higher cost.
Disclosure of Invention
The invention aims to provide a method for producing ethylenediamine tetraacetic nitrile (EDTN) and ethylenediamine tetraacetic acid (EDTA) by using hydroxyacetonitrile as a raw material through a one-pot method. The method simplifies the production process, improves the safety of production operation, and reduces the production cost such as energy consumption, equipment requirement, raw material consumption and the like.
The reaction formula of the method is as follows:
in a particular embodiment, for example, the process for preparing EDTN according to the invention comprises the following steps:
1) adjusting the pH of the ethylenediamine solution to 6-8 with concentrated hydrochloric acid or concentrated sulfuric acid, adding hydroxyacetonitrile to obtain ethylenediamine and hydroxyacetonitrile at a molar ratio of 1: 2-2.5, preferably about 1: 2, and reacting at 20-60 deg.C for 20 min to 1 hr to obtain ethylenediamine diacetonitrile as an intermediate;
2) heating to 60-100 deg.c, adding hydroxy acetonitrile in the molar ratio of 1 to 2-3, preferably 1 to 2.5, maintaining pH at 6 for 3-8 hr to produce ethylenediamine tetraacetic nitrile.
In another embodiment, for example, the process for the preparation of EDTA according to the invention comprises the following steps:
1) adjusting the pH of the ethylenediamine solution to 6-8 with concentrated hydrochloric acid or concentrated sulfuric acid, adding hydroxyacetonitrile to obtain ethylenediamine and hydroxyacetonitrile at a molar ratio of 1: 2-2.5, preferably about 1: 2, and reacting at 20-60 deg.C for 20 min to 1 hr to obtain ethylenediamine diacetonitrile as an intermediate;
2) heating to 60-100 deg.C, adding hydroxy acetonitrile, keeping the molar ratio of ethylenediamine diacetonitrile to hydroxy acetonitrile at 1: 2-3, preferably about 1: 2.5, keeping pH at about 6, reacting for 3-8 hr to obtain ethylenediamine tetraacetic nitrile, cooling, and vacuum filtering;
3) hydrolyzing ethylene diamine tetraacetic acid with alkali solution, controlling the reaction temperature at 40-105 ℃ and the reaction time at 2-6 hours to obtain ethylene diamine tetraacetic acid salt; acidifying with acid, and controlling pH to 1-3; filtering to obtain the ethylenediamine tetraacetic acid. Wherein the alkali is selected from sodium hydroxide, potassium hydroxide, sodium carbonate, potassium carbonate and mixtures thereof, preferably sodium hydroxide or potassium hydroxide with a concentration of 25-50%; the acid is selected from sulfuric acid, hydrochloric acid, phosphoric acid and mixtures thereof, preferably sulfuric acid or hydrochloric acid, more preferably sulfuric acid with a concentration of 40-60%.
Or hydrolyzing ethylene diamine tetraacetic acid with acid, controlling the pH value to be 1-3, controlling the reaction temperature to be 80-105 ℃, controlling the reaction time to be 2-6 hours, and filtering to obtain the ethylene diamine tetraacetic acid. The acid is sulfuric acid, hydrochloric acid, phosphoric acid and their mixture, preferably sulfuric acid or hydrochloric acid, more preferably 40-60% sulfuric acid.
In step 2) of the two processes according to the invention, the pH can be adjusted by customary methods, for example by saturated NaHCO3Or NaCO3And (3) solution. The pH adjustment may be carried out after the hydroxyacetonitrile has been reacted with ethylenediamine diacetonitrile for a certain period of time, and it is preferable to keep the reaction at this pH for 2 to 4 hours after the pH adjustment to about 6.
The hydroxyacetonitrile used in the method can be obtained by directly absorbing hydrogen cyanide with industrial formaldehyde, and the concentration of the hydroxyacetonitrile without purification is 0.2-0.7 g/ml. Since the hydroxyacetonitrile is easy to polymerize at high temperature and in a strong alkaline medium, and the too strong acidity can slow down the reaction speed of the hydroxyacetonitrile and the ethylenediamine, further increasing the side reaction degree of the polymerization of the hydroxyacetonitrile, the selection of proper temperature and pH value is the key for success. Through a series of researches on the temperature and the pH value of the method, the method disclosed by the invention has the advantages that in the method, the optimum temperature of the reaction for generating the ethylene diamine tetraacetic acid nitrile from the ethylenediamine diacetonitrile in the step 2) is 60-100 ℃, and the optimum pH value is about 6. The yield of the step reaches 78.5 to 85 percent.
Detailed Description
Example 1
In a three-necked round-bottomed flask equipped with a thermometer, a reflux condenser and a constant-pressure dropping funnel, 6.7ml (6g, 0.1mol) of ethylenediamine solution was adjusted to pH 6 to 8 with concentrated hydrochloric acid, 30ml (0.2mol) of hydroxyacetonitrile was added dropwise at room temperature, the temperature was raised to 40 ℃ to 50 ℃ and the temperature was maintained at 20 ℃ to 60 ℃ to react for 30 minutes or more (total 1 hour of dropwise addition and reaction). Heating to 60-100 ℃, dropwise adding 34ml (0.24mol) of hydroxy acetonitrile, reacting for 3 hours at 60-100 ℃, and then adding saturated NaHCO3The pH was adjusted to about 6 and the reaction was continued for 3 hours. Cooling, suction filtering, washing and drying to obtain EDTN 18.4g (85% yield) with a melting point of 132-.
Dissolving 5.4g (25mmol) of EDTN obtained above in 10.3ml of 30% NaOH solution, stirring for 30min at 40 ℃, heating to slightly boil, removing most ammonia for 4-5 hours, adding 5% of activated carbon for decolorization, performing suction filtration, acidifying with concentrated hydrochloric acid to pH 1.5, performing suction filtration, washing and drying to obtain 7g of EDTA (yield 96%).
The overall yield was 81.6%.
Claims (6)
1. A method for producing ethylene diamine tetraacetic acid acetonitrile by taking hydroxyl acetonitrile as a raw material is characterized by comprising the following steps:
1) adjusting the pH value of the ethylenediamine solution to 6-8 by using concentrated hydrochloric acid or concentrated sulfuric acid, adding hydroxy acetonitrile, and reacting at the temperature of 20-60 ℃ for 20 minutes to 1 hour to generate an intermediate product, namely ethylenediamine diacetonitrile;
2) heating to 60-100 deg.c, adding hydroxy acetonitrile and maintaining pH at 6 for 3-8 hr.
2. The process according to claim 1, wherein the molar ratio of ethylenediamine to hydroxyacetonitrile in step 1) is from 1: 2 to 2.5; in the step 2), the molar ratio of the ethylenediamine diacetonitrile to the hydroxyacetonitrile is 1: 2-3.
3. The process according to claim 1 or 2, wherein the concentration of the hydroxyacetonitrile is from 0.2 to 0.7 g/ml.
4. A method for producing ethylene diamine tetraacetic acid by taking hydroxyacetonitrile as a raw material is characterized by comprising the following steps:
1) adjusting the pH value of the ethylenediamine solution to 6-8 by using concentrated hydrochloric acid or concentrated sulfuric acid, adding hydroxy acetonitrile, and reacting at the temperature of 20-60 ℃ for 20 minutes to 1 hour to generate an intermediate product, namely ethylenediamine diacetonitrile;
2) heating to 60-100 ℃, adding hydroxy acetonitrile, keeping the pH value at about 6, and reacting for 3-8 hours;
3) hydrolyzing the ethylene diamine tetraacetic acid with alkali solution, controlling the reaction temperature at 40-105 ℃ and the reaction time at 2-6 hours to obtain ethylene diamine tetraacetic acid salt; acidifying with acid, and controlling pH to 1-3; filtering to obtain ethylenediamine tetraacetic acid; or hydrolyzing ethylene diamine tetraacetic acid with acid, controlling the pH value to be 1-3, controlling the reaction temperature to be 80-105 ℃, controlling the reaction time to be 2-6 hours, and filtering to obtain the ethylene diamine tetraacetic acid.
5. The process according to claim 4, wherein the molar ratio of ethylenediamine to hydroxyacetonitrile in step 1) is from 1: 2 to 2.5; in the step 2), the molar ratio of the ethylenediamine diacetonitrile to the hydroxyacetonitrile is 1: 2-3.
6. The process according to claim 4 or 5, wherein the concentration of the hydroxyacetonitrile is from 0.2 to 0.7 g/ml.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB200410069103XA CN1317261C (en) | 2004-07-05 | 2004-07-05 | Method of preparing ethylenediamine tetracetonitrile and ethylenediamine tetraacetic acid using hydroxy acetonitrile as raw material |
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB200410069103XA CN1317261C (en) | 2004-07-05 | 2004-07-05 | Method of preparing ethylenediamine tetracetonitrile and ethylenediamine tetraacetic acid using hydroxy acetonitrile as raw material |
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| CN1718569A true CN1718569A (en) | 2006-01-11 |
| CN1317261C CN1317261C (en) | 2007-05-23 |
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Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101723842B (en) * | 2009-11-06 | 2012-11-07 | 重庆紫光鼎福化工有限责任公司 | Method for preparing ethylene diamine tetraacetic acid (EDTA) disodium salt |
| CN102875400A (en) * | 2012-09-21 | 2013-01-16 | 烟台万华聚氨酯股份有限公司 | Diethylenetriamine pentaacetic acid preparation method |
| CN113444115A (en) * | 2020-03-27 | 2021-09-28 | 石家庄圣泰化工有限公司 | Synthesis method of methyl iminodiacetate of methyl borate |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5459228A (en) * | 1977-10-17 | 1979-05-12 | Showa Denko Kk | Preparation of ethylenediamine diacetonitrile |
| JPS5459224A (en) * | 1977-10-17 | 1979-05-12 | Showa Denko Kk | Preparation of ethylenediaminetetraacetates |
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2004
- 2004-07-05 CN CNB200410069103XA patent/CN1317261C/en not_active Expired - Fee Related
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101723842B (en) * | 2009-11-06 | 2012-11-07 | 重庆紫光鼎福化工有限责任公司 | Method for preparing ethylene diamine tetraacetic acid (EDTA) disodium salt |
| CN102875400A (en) * | 2012-09-21 | 2013-01-16 | 烟台万华聚氨酯股份有限公司 | Diethylenetriamine pentaacetic acid preparation method |
| CN113444115A (en) * | 2020-03-27 | 2021-09-28 | 石家庄圣泰化工有限公司 | Synthesis method of methyl iminodiacetate of methyl borate |
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| CN1317261C (en) | 2007-05-23 |
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Granted publication date: 20070523 Termination date: 20120705 |