Preparation process of N-(2-acetamido)-2-iminodiacetic acid

A technology of iminodiacetic acid and acetamide, which is applied in the field of preparation technology of N--2-iminodiacetic acid, can solve the problems of ADA being expensive and rare, and achieve shortened reaction production cycle, easy control, and reaction The effect of mild conditions

Active Publication Date: 2020-11-10
SUZHOU YACOO SCI CO LTD
View PDF4 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

This patented technology allows for more efficient methods of producing neodymium ammonia dyes that are less expensive than existing ones while maintain their quality or performance compared to current technologies such as dichloroacetic acids. It achieves this by reducing costs associated with raw material use without sacrificing its desired properties like color intensity or stability during storage over time. Additionally, it simplifies the manufacturing processes used in these molecules making them easier to operate at large scales. Overall, this innovative approach makes possible better ways to produce higher levels of nitrogen oxide compounds called ADAs.

Problems solved by technology

The technical problem addressed in this patented text relates to finding an efficient way to make certain types of chemicals called ADIA that can be useful as a substitute or supplementing other substances found naturally occurring within our environment (such as sulfur dioxide).

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Preparation process of N-(2-acetamido)-2-iminodiacetic acid
  • Preparation process of N-(2-acetamido)-2-iminodiacetic acid
  • Preparation process of N-(2-acetamido)-2-iminodiacetic acid

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0040] A kind of preparation technology of N-(2-acetamido)-2-iminodiacetic acid (ADA), comprising:

[0041] Step 1: In the reactor, in the presence of the reaction solvent acetonitrile, add ammonia water and methyl chloroacetate at a molar ratio of 1:1, set the reaction temperature to 20°C, and the reaction pressure to normal pressure. After 8 hours, the reaction is complete, and Intermediate products, as follows:

[0042]

[0043] Then spin off the solvent acetonitrile, add ethyl acetate, wash twice with water, dry over anhydrous sodium sulfate, then spin off the ethyl acetate to obtain an intermediate product with higher purity, the yield of the intermediate product is calculated to be 80%.

[0044]Step 2: In the presence of the reaction solvent acetonitrile, add amination reagent ammonia water to the reactor to react with the intermediate product obtained in step 1, wherein the molar ratio of ammonia water to the intermediate product is 1:1, and the reaction temperature is

Embodiment 2

[0054] A kind of preparation technology of N-(2-acetamido)-2-iminodiacetic acid (ADA), comprising:

[0055] Step 1: In the reactor, in the presence of the reaction solvent tetrahydrofuran, add ammonium chloride and chloroacetic acid at a molar ratio of 1:1, set the reaction temperature to 20°C, and the reaction pressure to normal pressure. After 8 hours, the reaction is complete, and Intermediate products, as follows:

[0056]

[0057] Then the solvent tetrahydrofuran was spun off, ethyl acetate was added, washed twice with water, dried over anhydrous sodium sulfate, and then the ethyl acetate was spun off to obtain an intermediate product with higher purity. The yield of the intermediate product was calculated to be 70%.

[0058] Step 2: In the presence of the solvent tetrahydrofuran, add ammonia as an aminating reagent to the reactor to react with the intermediate product obtained in step 1, wherein the molar ratio of ammonia water to the intermediate product is 1:1, and the

Embodiment 3

[0068] A kind of preparation technology of N-(2-acetamido)-2-iminodiacetic acid (ADA), comprising:

[0069] Step 1: In the reactor, in the presence of the reaction solvent methanol, add ammonium nitrate and ethyl chloroacetate at a molar ratio of 1:1, set the reaction temperature to 20°C, and the reaction pressure to normal pressure, and the reaction is completed after 8 hours. An intermediate product is generated, as follows:

[0070]

[0071] Then the solvent methanol was spun off, ethyl acetate was added, washed twice with water, dried over anhydrous sodium sulfate, and then ethyl acetate was spun off to obtain an intermediate product with higher purity. The yield of the intermediate product was calculated to be 85%.

[0072] Step 2: In the presence of solvent methanol, add amination reagent ammonia water to the reactor to react with the intermediate product obtained in step 1, wherein the molar ratio of ammonia water to intermediate product is 1:1, and the reaction tempera

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

PUM

No PUM Login to view more

Abstract

The invention discloses a preparation process of N-(2-acetamido)-2-iminodiacetic acid. The preparation process comprises the following steps: subjecting a reactant 1 with a structure as shown in a formula as described in the specification to reacting with a nitrogen-containing compound, and subjecting the obtained intermediate product to reacting with an amination reagent to obtain N-(2-acetamido)-2-iminodiacetic acid. In the formula, Y, Y1, Y2 and Y3 are respectively one selected from the group consisting of OH, OM, halogen, OR and SR; and Z is one selected from the group consisting of halogen, OH and SH. According to the invention, low-price starting raw materials are used, so cost can be greatly reduced; reaction conditions are mild, a subsequent purification process is simple, and theyield of N-(2-acetamido)-2-iminodiacetic acid is high; and the whole process disclosed by the invention is relatively simple to operate and easy to control, is beneficial for scale-up production, shortens the reaction production period, and is also beneficial to academic research and the like of N-(2-acetamido)-2-iminodiacetic acid.

Description

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Application Information

Patent Timeline
no application Login to view more
Owner SUZHOU YACOO SCI CO LTD
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products