Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Preparation method of isobutyramide

A technology of isobutyramide and isobutyronitrile, which is applied in the field of isobutyramide preparation, can solve the problems of difficult environmental protection requirements, increasing the difficulty of isobutyramide, and increasing the probability of containing harmful substances.

Inactive Publication Date: 2017-02-15
张敏
View PDF0 Cites 1 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Although the product purity of the isobutyramide obtained by this method for preparing isobutyramide has reached 99.87%, this method has the following disadvantages: the first is because the isobutyryl chloride used is very easy to react with water, in order to avoid Isobutyryl chloride decomposes in contact with water and other substances, and the solvent and other raw materials need to be strictly dewatered, and the reaction equipment needs to be strictly sealed. The reaction process of isobutyryl chloride and ammonia is extremely violent, so the control of the reaction conditions is also very demanding. Strict, these increase the difficulty of preparing isobutyramide
These result in more treatment of the three wastes, it is difficult to meet the requirements of environmental protection, and the cost of production is increased.
The 3rd is that this method process is complicated, and the yield of product is low, has only about 88%, and has used benzene organic solvent in the preparation process, makes the probability increase that contains harmful substance in the product, is exactly the extremely trace amount of organic solvent in different The presence of butanamide also has a great adverse effect on the application of the product in the medical field

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 method of isobutyramide

Examples

Experimental program
Comparison scheme
Effect test

Embodiment Construction

[0023] The implementation of the composite window control platform based on wind volume detection of the present invention will be described in detail below with reference to the accompanying drawings.

[0024] A preparation method of isobutyramide, the method comprising:

[0025] Carry out the following steps in the reactor in the smart factory:

[0026] (1): The treatment of nitrile hydratase catalyst: the fermented liquid obtained by fermenting the nitrile hydratase production strain is separated with a 1.5mm sintered metal filter, and then cleaned twice with deionized water, and the strain is star-shaped Nocardia ATCC 19247;

[0027] (2): Preparation of isobutyramide by hydration of isobutyronitrile: adding the cleaned nitrile hydratase catalyst to deionized water, the mass ratio of the amount of nitrile hydratase catalyst added to the amount of deionized water added is 0.02:1, isobutyramide The mass ratio of the amount of nitrile added to the amount of deionized water a...

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 relates to a preparation method of isobutyramide. The method comprises the following steps: conducting a hydration reaction of isobutyronitrile and de-ionized water, which serve as raw materials, under the action of a nitrile hydratase catalyst so as to obtain isobutyramide, and conducting simple treatment on an obtained isobutyramide water solution so as to obtain a high-purity isobutyramide crystal product. According to the preparation method provided by the invention, the high-purity isobutyramide crystal product can be prepared by conducting simple treatment on the obtained isobutyramide water solution; and the product, which is higher than 99.95% in purity and is free from such harmful ingredients as an organic solvent and the like, is especially applicable to medical field. The method is mild in reaction conditions and simple to operate, simple in preparation process and easy for industrialization, and the yield of the product reaches 99% or above.

Description

technical field [0001] The invention relates to the field of chemical industry, in particular, the invention relates to a preparation method of isobutyramide. Background technique [0002] Isobutyramide can selectively induce human g-globin gene transcription, coupled with the non-toxicity of isobutyramide and the longer half-life in plasma, it makes isobutyramide ideal in the treatment of b-thalassemia and sickle cell anemia Effect. Isobutyramide is also an important intermediate in the synthesis of ritonavir, a drug for the treatment of AIDS. Isobutyramide is widely used in the field of medicine, and the research on various intermediates used in its preparation process and isobutyramide is becoming a hot spot in this field. [0003] There have been some reports on the production and preparation methods of isobutyramide, mainly based on the method of reacting isobutyryl chloride and ammonia. The representative method is the preparation method of isobutyramide proposed by ...

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
Patent Type & Authority Applications(China)
IPC IPC(8): C12P13/02G05B19/042C12R1/365
CPCC12P13/02G05B19/042
Inventor 沈源张瀚文朱文明
Owner 张敏
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products