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

Preparation method of p-nitrobenzaldehyde

A technology of p-nitrobenzaldehyde and p-nitrobenzyl alcohol, applied in the field of preparation of known compounds, can solve the problems of no obvious advantages in production cost and industrial operation, expensive catalyst, difficult recovery and regeneration, etc. The effect of industrial preparation reaction operation safety, reduction of industrial preparation costs, and reduction of organic by-products

Inactive Publication Date: 2016-02-24
NANJING UNIV OF SCI & TECH
View PDF1 Cites 5 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Liu Changchun and others applied this method to the synthesis of p-nitrobenzaldehyde, using RuHAP as a catalyst, oxygen oxidation of p-nitrobenzyl alcohol under normal pressure to prepare p-nitrobenzaldehyde, this method can significantly improve the synthesis of p-nitrobenzaldehyde Selectivity and increase product yield, but the catalyst is expensive and difficult to recycle and recycle
Peng Xinhua et al. used p-nitrotoluene as a raw material, reacted with bromine to form p-nitrobenzyl bromide, then catalyzed hydrolysis by sodium carbonate to form p-nitrobenzyl alcohol, and further synthesized p-nitrobenzene by oxygen oxidation catalyzed by metal-organic complexes. Formaldehyde, although significantly improved reaction selectivity, has improved productive rate, but the organic peroxide liquid catalyst of bromination reaction procedure, its thermal stability of industrial application is poor; The used metal organic complex catalyst of the 3rd step oxidation reaction procedure is difficult Regeneration, and oxygen oxidation is a gas-liquid phase reaction system, which needs to be reacted under certain pressure conditions. Therefore, there is no obvious advantage in production costs and industrial operations.

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 p-nitrobenzaldehyde
  • Preparation method of p-nitrobenzaldehyde
  • Preparation method of p-nitrobenzaldehyde

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0027] In the reactor, add 80g chlorobenzene, 13.7g p-nitrotoluene, 2.7g azobisisovaleronitrile, slowly add 9.6g bromine dropwise within 30min at 50°C, after the dropwise addition, stir and heat to reflux React until the bromine color fades. Slowly add 7.0 g of 27.5% hydrogen peroxide dropwise within 30 min, and stir and reflux for 3 h. Add 68.5g of 20% potassium carbonate aqueous solution to the reaction solution, stir and reflux for 30h, recover chlorobenzene by distillation, cool and stand to separate the water phase and the organic phase containing p-nitrobenzyl alcohol. Transfer the organic phase into the reactor, add 2.7g of sodium hydroxide, stir and control the temperature at 25°C, add 48.7g of 35% hydrogen peroxide dropwise within 30min, and heat to reflux for 26h. After the reaction was completed, it was cooled to room temperature, and the organic phase was separated by standing. After washing, the organic solvent was concentrated, and 11.5 g of p-nitrobenzaldehyde ...

Embodiment 2

[0029] In the reactor, add 80g of chlorobenzene, 13.7g of p-nitrotoluene, and 1.2g of azobisisoheptanonitrile, and slowly add 9.0g of bromine dropwise within 30min at 45°C. After the dropwise addition, stir and heat to reflux React until the bromine color fades. Slowly add 7.0 g of 27.5% hydrogen peroxide dropwise within 30 min, and stir and reflux for 2 h. Add 41.5 g of 30% potassium carbonate aqueous solution to the reaction solution, stir and reflux for 21 h, recover chlorobenzene by distillation, and cool and stand to separate the water phase and the organic phase containing p-nitrobenzyl alcohol. Transfer the organic phase into the reactor, add 1.5g of sodium hydroxide, stir and control the temperature at 30°C, add 62.0g of 27.5% hydrogen peroxide dropwise within 30min, and heat to reflux for 26h. After the reaction was completed, cool to room temperature, stand to separate the organic phase, concentrate the organic solvent after washing, and refine with ethanol to obtai...

Embodiment 3

[0031]In the reactor, add 80g of o-dichlorobenzene, 13.7g of p-nitrotoluene, and 1.2g of azobisisooctanonitrile, and slowly add 9.0g of bromine dropwise within 30min at 45°C. After the dropwise addition, stir and heat The reaction was refluxed until the color of bromine faded. Slowly add 7.0 g of 27.5% hydrogen peroxide dropwise within 30 min, and stir and reflux for 2 h. Add 41.5 g of 30% potassium carbonate aqueous solution to the reaction solution, stir and reflux for 23 hours, recover o-dichlorobenzene by distillation, and cool and stand to separate the water phase and the organic phase containing p-nitrobenzyl alcohol. Transfer the organic phase into the reactor, add 1.5g of sodium hydroxide, stir and control the temperature at 30°C, add 34.1g of 50% hydrogen peroxide dropwise within 30min, and heat to reflux for 26h. After the reaction was completed, cool to room temperature, stand to separate the organic phase, concentrate the organic solvent after washing, and refine ...

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-nitrobenzaldehyde. The preparation method comprises the following steps: p-nitrotoluene, which is used as a raw material, undergoes bromine bromination under the catalysis of azo-dialkyl nitrile, so as to generate 4-nitrobenzyl bromide and hydrogen bromide; hydrolysis of 4-nitrobenzyl bromide is catalyzed by an aqueous carbonate solution to obtain p-nitrobenzyl alcohol; and hydrogen peroxide oxidation of p-nitrobenzyl alcohol is catalyzed by sodium hydroxide so as to generate a target product, namely p-nitrobenzaldehyde. According to the invention, the azo-dialkyl nitrile solid catalyst replaces a peroxycarbonate liquid phase catalyst to catalyze the bromination reaction, so as to raise operational safety of the industrial preparation reaction; by using aryl halide as a solvent medium, use of a haloalkane solvent medium is avoided, and pollution of volatile organic solvents with low boiling point is avoided; and by the hydrogen peroxide oxidation method, cleanliness of the industrial preparation reaction is raised, and environmental pollution is reduced. According to the invention, product yield is increased; yield is raised by about 3% in comparison with yield of existing traditional industrial methods; overall yield reaches 76%; and product purity reaches 99% and above.

Description

technical field [0001] The present invention relates to a kind of preparation method of known compound, is exactly a kind of industrial clean preparation method of p-nitrobenzaldehyde. Background technique [0002] p-Nitrobenzaldehyde is a light yellow crystalline powder with a melting point of 105-107°C. It is slightly soluble in water and soluble in organic solvents such as alcohols, aromatics, halogenated hydrocarbons, and carboxylates. Vapor volatility properties. Molecular formula is C 7 h 5 NO 3 , relative molecular mass 151.1. Its structural formula is: [0003] [0004] p-Nitrobenzaldehyde is used as an important intermediate in the synthesis of fine organic functional materials such as medicines, dyes, and pesticides. It has a wide range of uses and can derive many important functional chemicals. In the field of important intermediates used in the synthesis of pesticides, medicines, dyes, photosensitive materials and liquid crystal materials, such as the p...

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): C07C205/44C07C205/11C07C201/12
Inventor 彭新华马庆国徐俊辉
Owner NANJING UNIV OF SCI & TECH
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