A kind of preparation method of p-methylthiobenzaldehyde

A technology for p-chlorobenzaldehyde and benzaldehyde, which is applied in sulfide preparation, mercaptan preparation, organic chemistry and other directions, can solve the problems of increasing the difficulty of wastewater treatment, a large number of organic impurities, poor operating conditions, etc., and achieves high product yield, The effect of high total yield and good industrialization prospects

Active Publication Date: 2021-07-23
SHANDONG GUOBANG PHARMA +1
View PDF0 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

But, be applied to bromine in the method (1), produce hydrobromic acid, have a large amount of waste acid to produce, and reaction is a high-temperature reaction, can produce a large amount of organic impurities in the production process, increased the wastewater treatment difficulty, simultaneously bromine is in production and There are certain safety risks in the transportation process, and the overall yield is only about 85%, and the cost is relatively high; method (2) has a simple reaction process, mild reaction conditions, and the overall yield can reach 88~92%, but in the first step In the reaction, sodium methyl mercaptide, which is one of the main raw materials, is easily hydrolyzed to release foul smell and extremely low threshold value of methyl mercaptan gas, which will inevitably produce foul smell and toxic pollutants, which has a great impact on the environment, and the operating conditions are relatively low. Difference

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
  • A kind of preparation method of p-methylthiobenzaldehyde
  • A kind of preparation method of p-methylthiobenzaldehyde

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0028] a. Take 412g (0.261mol) of 10% sodium thiosulfate solution and add it to a four-necked flask with mechanical stirring, add 0.63g (0.00227mol) tetrabutylammonium chloride, raise the temperature to 70°C, and throw in 31.95 g (0.227mol) p-chlorobenzaldehyde, reacted for 4 hours;

[0029] b. Add concentrated sulfuric acid to adjust pH=0, heat up to 90°C, and keep warm for 2 hours; then lower the temperature to 60°C, add 0.15g zinc powder, stir and keep warm for 2 hours; then add 32% liquid alkali dropwise to adjust pH=9.0, Stir for 1 hour;

[0030] c. Put the material into the autoclave, raise the temperature to 90°C, feed in methyl chloride, keep the pressure in the kettle at 0.5MPa, and keep it warm for 8 hours; after the heat preservation is over, cool it to 35°C, and put the material into the separatory funnel to stand still After 30 minutes, the lower organic phase was collected to obtain the product crude product; 31.95g sodium sulfate was added to absorb water in th...

Embodiment 2

[0032] The difference between this implementation method and Example 1 is that the phase transfer catalyst is the tetrabutylammonium bromide of 0.73g (0.00226mol), and other steps are identical, obtain 33.79g product, molar yield 97.70%, gas phase detection purity is 99.3%.

Embodiment 3

[0034] The difference between this implementation method and Example 1 is that the phase transfer catalyst is 0.67g (0.00227mol) tetrabutyl chloride Other steps are the same, 32.86g product is obtained, the molar yield is 95.03%, and the gas phase detection purity is 99.2%.

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 method of p-methylthiobenzaldehyde. Sodium thiosulfate is used to replace sodium methylthiolate to generate bunte salt, and then p-methylthiobenzaldehyde is synthesized through acid hydrolysis and methylation reaction. The invention avoids the disadvantages of using sodium methyl mercaptide as a substitute in the existing production process line, effectively solves the odor problem in the use process of sodium methyl mercaptide, and the raw materials are cheap and easy to obtain, clean and pollution-free, and the operation process is simple. The yield is high and has good industrialization prospects.

Description

technical field [0001] The invention belongs to the technical field of organic chemical synthesis, and also belongs to the technical field of synthesis of veterinary drugs and pharmaceutical raw materials, and relates to a method for synthesizing p-methylthiobenzaldehyde, an intermediate p-methylsulfonylbenzaldehyde, which is a raw material of florfenicol. Background technique [0002] Florfenicol (Florfenicol, also known as fluprofen, fluthiamphenicol) is a white or off-white crystalline powder, odorless, and bitter in taste. It is a new veterinary special chlorine that was successfully developed in the late eighties. Broad-spectrum antimicrobials. The main raw material of Florfenicol is D-p-thymphenylphenylserine ethyl ester (commonly known as D-ethyl ester). [0003] The synthesis of D-ethyl ester takes p-thymphenyl benzaldehyde as raw material, and there are two methods for p-thymphenyl benzaldehyde: (1) using p-thymphenyl toluene as the starting material, reacting with...

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): C07C319/14C07C323/22
CPCC07C319/02C07C319/14C07C381/02C07C323/22
Inventor 张小垒刘聪赵肖泽王召平
Owner SHANDONG GUOBANG PHARMA
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