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

Synthesis method for 4-bromo-2, 6-difluoro-trifluoromethoxybenzene

A technology for the synthesis of trifluoromethoxybenzene and its synthesis method, which is applied to the synthesis of 4-bromo-2,6-difluoro-trifluoromethoxybenzene and the field of intermediate synthesis, and can solve the problems that are not suitable for industrial production and synthesis. Problems such as short routes and highly toxic hydrogen fluoride have achieved the effects of being conducive to industrial production, short synthesis routes, and reducing environmental pressure

Active Publication Date: 2012-07-04
河北凡克新材料有限公司
View PDF4 Cites 8 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

This method has a short synthetic route and a high yield, but the starting material 2,6-difluorophenol is not easy to purchase, and generally needs to be self-made, and the high price makes the production cost higher. Hydrogen fluoride is highly toxic and highly corrosive, and is not easy to popularize. Suitable for industrial production

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
  • Synthesis method for 4-bromo-2, 6-difluoro-trifluoromethoxybenzene
  • Synthesis method for 4-bromo-2, 6-difluoro-trifluoromethoxybenzene

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0024] In a 250 ml three-necked flask, add 0.2 mol (42.2 g) of 3,4,5-trifluorobromobenzene, stir, and start to add 57.9 g of 28% sodium methoxide (0.3 mol) methanol solution dropwise at room temperature. Reflux, reaction 6h. After the reaction is complete, filter off the solid, remove the solvent by rotary evaporation of the filtrate, add 50ml of water and 80ml of 1,2-dichloroethane to the residue, separate the layers, wash the organic phase with water until neutral, add 4.0g of anhydrous magnesium sulfate to dry, and filter with suction , the filtrate was rotary evaporated to remove the solvent, the residue was subjected to vacuum distillation, and 41.6 g of fractions at 92~93°C / 15mmHg were collected, with a yield of 93.3%.

Embodiment 2

[0026] In a 250 ml three-necked flask, add 0.2mol (42.2g) of 3,4,5-trifluorobromobenzene, 1.25mol (40.0g) of anhydrous methanol, stir, and start adding 0.3mol (12.5 g) 96% sodium hydroxide, after the addition, the temperature was raised to reflux, and the reaction was carried out for 7 hours. After the reaction is completed, filter, remove the solvent by rotary evaporation of the filtrate, add 50ml of water and 80ml of 1,2-dichloroethane to the residue to separate the liquid, wash the organic phase with water until neutral, add 4.0g of anhydrous magnesium sulfate to dry, filter with suction, and spin the filtrate The solvent was removed by evaporation, and the residue was rectified under reduced pressure to collect 42.4 g of fractions at 92-94°C / 15mmHg, with a yield of 95.1%.

[0027] 2. Synthesis of compound II 4-bromo-2,6-difluorophenetole

[0028] Example 1

[0029] In a 250 ml three-necked flask, add 0.28 mol (19.1 g) of sodium ethoxide and 80 ml of toluene, stir, and st...

Embodiment 3

[0038]In a 250 ml three-necked flask, add 0.1mol (23.7g) 4-bromo-2,6-difluorophenetole, 21.9g DMF, stir, add 0.15mol (6.4g) lithium chloride, after the addition is complete, heat up to reflux , Reaction 5h. After the reaction is complete, pour the reaction solution into a mixture of ice and water, extract with 50ml of toluene, separate the layers, wash the organic phase with water until neutral, add 2.0g of anhydrous magnesium sulfate to dry, filter with suction, remove the solvent by rotary evaporation of the filtrate, and depressurize the residue Rectification, collecting 18.3g fraction at 71~74℃ / 8mmHg, yield 87.6%, gas phase monitoring, purity 99.05%.

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 synthesis method for 4-bromo-2, 6-difluoro-trifluoromethoxybenzene adopts 3, 4, 5-trifluorobromobenzene(I) as material and sequentially carries out substitution, dealkylation and trifluoromethylation reactions to prepare 4-bromo-2, 6-difluoro-trifluoromethoxybenzene (IV). The method has the advantages of short synthesis route, high yield, low cost, easy industrialization and the like.

Description

technical field [0001] The present invention relates to a synthetic method of an intermediate, in particular to a synthetic method of 4-bromo-2,6-difluoro-trifluoromethoxybenzene which can be effectively used as an intermediate of liquid crystal display materials, belonging to the chemical synthetic field. Background technique [0002] 4-Bromo-2,6-difluoro-trifluoromethoxybenzene is an increasingly versatile intermediate for the synthesis of liquid crystal compounds. [0003] A synthetic route of 4-bromo-2,6-difluoro-trifluoromethoxybenzene is disclosed in German Patent DE4221152, as shown in the following formula (B): [0004] [0005] The method is characterized in that 2,6-difluoro-trifluoromethoxybenzene is nitrated at the 3-position with nitric acid and sulfuric acid; then the nitro group is reduced into an amino group in the presence of a transition metal catalyst and hydrogen; Under the action of 4-bromo; finally deamination in the presence of tert-butyl nitrite ...

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
IPC IPC(8): C07C43/225C07C41/16
CPCY02P20/582
Inventor 李韶辉师俊杰陆敬国周文涛司晓芳林艳艳段军
Owner 河北凡克新材料有限公司
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

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

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com