Process of producing nitrobenzether aminobenzether amidobenzether from chlorobenzene

A technology of amidophenylene ether and nitrophenylene ether, which is applied in the preparation of amino hydroxyl compounds, nitro compounds, carboxylic acid amides, etc., can solve the problems of large amount of three wastes, difficulty in treatment, high separation cost, etc., and achieve production cost Low, high production stability and safety effect

Inactive Publication Date: 2009-06-03
CHANGZHOU JIASEN CHEM +1
View PDF7 Cites 4 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] The purpose of the present invention is to provide a short process flow, fast reaction speed, high selectivity, simple separation process and low production cost in view of the high investment, high separation cost, large amount of three wastes and difficult treatment in the current production process. A process for producing nitrophenyl ether, aminophenyl ether and amidophenyl ether from chlorobenzene, which is safe and reliable, and has no three wastes in the production process

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
  • Process of producing nitrobenzether aminobenzether amidobenzether from chlorobenzene
  • Process of producing nitrobenzether aminobenzether amidobenzether from chlorobenzene
  • Process of producing nitrobenzether aminobenzether amidobenzether from chlorobenzene

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0052] A clean production of o-nitroanisole, p-nitroanisole, anthranil, p-aminoanisole, 2,4-dinitroanisole, 2,4- The technique of diaminoanisole and 2-amino-4-acetamidoanisole, described processing step is as follows:

[0053] (1). Nitration reaction, using chlorobenzene as raw material, chlorobenzene is subjected to adiabatic nitration by mixed acid composed of nitric acid and sulfuric acid in a static mixed nitration reactor to obtain a mixture of nitrochlorobenzene, and the dehydration value of the mixed acid is between 2.0-3.2 Between, the ratio of chlorobenzene to nitric acid is 1:1.05. Continuous adiabatic nitration reaction occurs in continuous static mixer adiabatic nitration reactor. mixed with water

[0054] (2). Evaporation and concentration, after continuous adiabatic nitration reaction, the material is decompressed to 98.0kPa, water and residual nitric acid are distilled off, and then liquid-liquid separation;

[0055] (3). Liquid-liquid separation. The evaporat...

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

A process for preparing nitrophenylether, aminophenylether and amidophenylether between chlorobenzene and acid mixture removing water, liquid-liquid separation to obtain organic phase consisting of o-, p- and meta-nitro chlorobenzene compounds, etherifying said mixture, recovering etherifying agent, vacuum distilling, separating and refining meta-nitro chlorobenzene, removing chloride salt generated in etherification, crystallizing separation, recrystallizing p- and o-nitro phenylether compounds, catalytic hydrogenating reaction, nitrifying reaction to obtain 2,4-drinitro phenylether, catalytic hydroreducing reaction to obtain 2,4-diamino phenylether, and aceylating reaction to obtain 2-amino-4-acetylamino phenylether.

Description

technical field [0001] The invention relates to a process for producing nitrophenyl ether, aminophenyl ether and amidophenyl ether with chlorobenzene, belonging to the technical field of fine chemicals. Background technique [0002] Nitrophenyl ether, aminophenyl ether and amidophenyl ether are important intermediates in industries such as dyes, medicines, and spices. [0003] Nitrophenyl ether, aminoanisole and amidoanisole (mainly o-nitroanisole, p-nitroanisole, o-aminoanisole, p-aminoanisole, 2,4-dinitrobenzene The traditional production method of methyl ether, 2,4-diaminoanisole, 2-amino-4-acetamidoanisole, etc.) mainly uses chlorobenzene as raw material, and produces nitrochlorobenzene mixture through mixed acid nitration reaction, nitro The chlorobenzene mixture is separated by rectification-crystallization to obtain the finished products of o-nitrochlorobenzene, m-nitrochlorobenzene and p-nitrochlorobenzene, and the etherification reaction of p-nitrochlorobenzene and...

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 Patents(China)
IPC IPC(8): C07C201/08C07C205/36C07C213/02C07C217/82C07C233/07C07C231/02
Inventor 许文林段玉辉刘学谦
Owner CHANGZHOU JIASEN CHEM
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

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap