Preparation method of 4,4'-difluorobenzophenone

A technology of difluorobenzophenone and difluorophenyl dichloromethane is applied in the field of preparation of 4,4'-difluorobenzophenone, and can solve the problem of unsatisfactory yield, difficult process control, many steps, etc. problem, to achieve the effect of low cost, good selectivity and high yield

CN106045828AActive Publication Date: 2016-10-26大连鼎燕医药化工有限公司
5 Cites 12 Cited by

Patent Information

Authority / Receiving Office
CN · China
Current Assignee / Owner
Publication Date
2016-10-26

Smart Images

  • Figure 1
    Figure 1
  • Figure 2
    Figure 2
  • Figure 3
    Figure 3
Patent Text Reader

Abstract

The invention relates to a preparation method of 4,4'-difluorobenzophenone, belonging to the field of chemical synthesis. The preparation method comprises the steps of carrying out acylation reaction on fluorine benzotrichloride and fluorobenzene under the catalysis of aluminum trichloride, and carrying out hydrolysis reaction, so as to obtain 4,4'-difluorobenzophenone. The preparation method of 4,4'-difluorobenzophenone has the beneficial effects of simple process, high yield, good selectivity and low cost.
Need to check novelty before this filing date? Find Prior Art

Description

technical field

[0001] The invention relates to a preparation method of 4,4'-difluorobenzophenone, which belongs to the field of chemical synthesis. Background technique

[0002] 4,4'-Difluorobenzophenone is the main intermediate for the preparation of engineering plastic polyether ether ketone (PEEK). Polyetheretherketone (PEEK) is a semi-crystalline aromatic plastic engineering plastic with high heat resistance, radiation resistance, corrosion resistance, high impact strength, good wear resistance and fatigue resistance, excellent flame retardancy and electrical properties With its excellent physical and mechanical properties, it can replace metals, ceramics and other materials in many fields. It is one of the most popular high-performance engineering plastics today. It has been widely used in various fields such as coatings and coatings, and has become an indispensable key material.

[0003] However, the preparation cost of 4,4'-difluorobenzophenone, the key intermediat...

Examples

Embodiment 1

[0035] A kind of preparation method of 4,4'-difluorobenzophenone, described preparation method comprises the steps:

[0036] ① Mix 200g of fluorobenzene and 65g of anhydrous aluminum trichloride, cool to 0-5°C, add 100g of p-fluorobenzotrichloride dropwise and react for 20min to obtain 4,4'-difluorophenyldichloromethane;

[0037] ②Add 4,4'-difluorophenylmethylene chloride to 600g of water and mix well, heat to azeotropic temperature and recover 140g of fluorobenzene, react for 5h, cool to room temperature, filter, dry to obtain 102g of light yellow solid crude product, use 200g of methanol was recrystallized, filtered, washed, and dried to obtain 92g of white crystals with a melting point of 107-108°C. The purity was 99.9% by gas chromatography, and the yield was 90%. through 1 H-NMR detection: δ7.28 (4H, t, hydrogen at the ortho-position of fluorine on the benzene ring); δ7.81 (4H, m, hydrogen at the ortho-position of carbonyl on the benzene ring), consistent with 4,4'-diflu...

Embodiment 2

[0039] A kind of preparation method of 4,4'-difluorobenzophenone, described preparation method comprises the steps:

[0040] ①Mix 100g of p-fluorobenzotrichloride and 200g of anhydrous fluorobenzene, cool to 0-5°C, add 70g of anhydrous aluminum chloride in batches and react for 20min to obtain 4,4'-difluorophenyldichloromethane ;

[0041] ②Add 4,4'-difluorophenyldichloromethane to 600g of water and mix well, heat to azeotropic temperature and recover 139.2g of fluorobenzene, react for 5h, cool to room temperature, filter and dry to obtain 102.8g of light yellow solid crude product , using 200g of methanol for recrystallization, filtering, washing, and drying to obtain 93g of white crystals with a melting point of 107-108°C, the purity of which was 99.9% by gas chromatography, and the yield was 91%. through 1 H-NMR detection: δ7.28 (4H, t, hydrogen at the ortho-position of fluorine on the benzene ring); δ7.81 (4H, m, hydrogen at the ortho-position of carbonyl on the benzene r...