Process for producing 4,4'-bisphenol sulphone

A manufacturing method and technology of phenol sulfone, applied in chemical instruments and methods, preparation of organic compounds, organic chemistry, etc., can solve the problems of no post-processing operation, difficult to deal with solid blocks, difficulties, etc., and achieve easy recycling and reuse. , The effect of promoting removal and easy reflow operation

Inactive Publication Date: 2007-08-22
NIPPON SODA CO LTD
View PDF9 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, there is a problem that the reaction product obtained after the solvent is distilled off becomes a solid block that is industrially difficult to handle, and it is necessary to control the reaction conditions for adjusting the removal rate of the solvent and the isomerization rate
In addition, in this invention, two types of solvents are used: a suspending agent (for example, AISOPA-(registered trademark of Exson Chemical Co., Ltd.) H, initial boiling point 176°C) and an entrainer (for example, AISOPA-E, initial boiling point 115°C) It is indispensable, but when using solvents with different physical properties as described above, the problem is that when the solvent is reused, it will be difficult to manage the boiling point, etc., and it will also lead to an increase in production costs.
[0011] Therefore, in above-mentioned prior art, also do not have the method that the aftertreatment operation after reaction is favorable

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 for producing 4,4'-bisphenol sulphone
  • Process for producing 4,4'-bisphenol sulphone

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0102] Put 98.7g (1.05mol) of phenol, 75ml of Aisopa-H, and 50ml of mesitylene into a 500ml four-necked flask equipped with a stirrer, a thermometer, and a water separation tube. 51.6 g (0.50 mol) of 95% sulfuric acid was added dropwise thereto, and then the temperature was raised.

[0103] Distillation of the reaction liquid started from around 148° C., the distillate was condensed in a water separation tube and separated into two layers, and the upper organic layer was continuously returned to the reaction system. The temperature of the reaction system reached 170° C. after about 4 hours from the start of the temperature rise, the generation of water stopped, and the amount of water separated in the water separation tube was 20.5 g. Thereafter, 50 ml of AISOPA-H was added, and it took 3 hours for the temperature of the reaction system to reach 175° C. to distill off mesitylene. The composition of the reactant was analyzed by high-performance liquid chromatography (HPLC), an...

Embodiment 2

[0107] 98.7 g (1.05 moles) of phenol and 100 ml of AISOPA-G were placed in a 500 ml four-neck flask equipped with a stirrer, a thermometer, and a water separation tube, and 95% sulfuric acid 51.6 g was added dropwise to the mixture at 50°C under stirring conditions. g (0.50 mol), the temperature was raised.

[0108] Distillation of the reaction liquid started at around 144°C, and the distillate was condensed and separated into three layers in a water separation tube. The upper layer was a solvent layer, the middle layer was a water layer, and the bottom layer was a phenol layer. The upper solvent layer was continuously returned to the reaction system, and the bottom phenol layer was extracted every 15 minutes and returned to the reaction system. The temperature of the reaction system reached 167° C. in about 7 hours from the start of the temperature rise, the generation of water stopped, and the amount of water separated in the water separation tube was 21.2 g. The total amou...

Embodiment 3

[0112] 117.5 g (1.25 moles) of phenol and 100 ml of Aysopa-G were placed in a 500 ml four-necked flask equipped with a stirrer, a thermometer, a water separation tube, and a Wedman-type rectification column, and the After 51.6 g (0.50 mol) of 95% sulfuric acid was added dropwise to the mixture, the temperature was raised.

[0113] Distillation of the reaction liquid started around 144°C, and the distillate was condensed and separated into three layers in the water separation tube, the upper layer being a solvent layer, the middle layer being a water layer, and the bottom layer being a phenol layer. The upper solvent layer was continuously returned to the reaction system, and the bottom phenol layer was reacted without returning to the reaction system. The temperature of the reaction system reached 167° C. in about 10 hours from the start of the temperature rise, and the generation of water stopped. The amount of water separated in the water separation tube was 20.5 g, and the ...

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

PropertyMeasurementUnit
boiling pointaaaaaaaaaa
boiling pointaaaaaaaaaa
boiling pointaaaaaaaaaa
Login to view more

Abstract

During reaction of phenol and sulfuric acid to produce 4, 4í»-bisphenol sulfone, the reaction system is dewatered in mixed solvent comprising saturated aliphatic hydrocarbon of boiling point not lower than 175 deg.c and mesitylene, and the reaction system is ultimately distilled to eliminate mesitylene. Or, the reaction is completed in solvent containing saturated aliphatic hydrocarbon inside a reaction container with rectifier, so as to obtain excellent operation performance and high yield of 4, 4í»-bisphenol sulfone. In addition, after reaction in solvent containing saturated aliphatic hydrocarbon, C1-C3 alcohol is added into the reacted solution, so that 4, 4í»-bisphenol sulfone is re-crystallized in separated alcohol layer and high purity 4, 4í»-bisphenol sulfone product is obtained simply.

Description

[0001] This application is a divisional application of a Chinese patent application with an application date of March 20, 2002 and an application number of 02828560.3 (international application number is PCT / JP02 / 02702). technical field [0002] The present invention relates to a method for producing 4,4'-bisphenol sulfone (or 4,4'-dihydroxydiphenylsulfone, hereinafter referred to as 4,4'-BPS) by reacting phenol and sulfuric acid. Background technique [0003] 4,4'-BPS is a useful compound generally used as a raw material for engineering plastics such as polysulfone (PSF) and polyethersulfone (PES). In order to produce this 4,4'-BPS, although the method of reacting phenol and sulfuric acid has been frequently studied, the main problems of this technology are how to efficiently remove water and how to reduce the by-product isomer 2,4 '-BPS to increase the yield of 4,4'-BPS in both ways. [0004] A kind of 4, the manufacture method of 4 '-BPS is disclosed in the Japanese Pate...

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): C07C317/22C07C315/00
Inventor 肥高友也
Owner NIPPON SODA 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

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